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intacsforkeratoconus.com

Intacs® Corneal Implants are ophthalmic medical devices designed for patients with keratoconus, reducing or postponing the needs for a corneal transplant

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What are Intacs corneal implants?

Intacs corneal implants are small, curved plastic segments (made from PMMA) that a surgeon inserts into the peripheral stroma of the cornea—roughly two-thirds deep, outside the central optical zone—through a small radial incision. According to the product's own description on Intacs - Intacs, Keratoconus Treatment, they are designed to reshape and stabilize a keratoconus cornea, reducing myopia and astigmatism so functional vision can be restored and a corneal transplant potentially deferred. The segments come in different thicknesses and are designed to be removable or replaceable.

Who it's for and how it fits into care

Keratoconus thins and bulges the cornea into a cone, distorting vision. Intacs is positioned as an option to improve vision before a transplant is considered—not as a cure for the underlying disease. A typical reader scenario: someone with keratoconus whose glasses or contact lenses no longer give usable vision, and who wants to explore surgical options short of transplantation.

Practical trade-offs to weigh

  • Goal is deferral, not cure: the stated aim is improving vision and postponing transplant, so expectations should match that.
  • Reversibility is a design feature: removability/replaceability matters if vision changes or another procedure is later needed.
  • Candidacy depends on the individual cornea: thickness, cone location and severity all influence whether this is appropriate, which only an eye-care professional can assess.

Next step

Ask a cornea specialist whether you fit the profile for intracorneal segments versus other options (such as corneal cross-linking or specialty contact lenses), and what the realistic vision outcome and follow-up would be. For broader context, the American Academy of Ophthalmology and National Eye Institute publish patient-oriented material on keratoconus and its treatments.

How do Intacs implants improve vision in people with keratoconus?

Intacs corneal implants are small arc-shaped segments placed in the outer layer of the cornea, outside the central optical zone. In keratoconus, the cornea thins and bulges into a cone, distorting vision. According to Intacs - Intacs, Keratoconus Treatment, inserting these segments reshapes and stabilizes the cornea, which can reduce or eliminate the myopia and astigmatism caused by the condition and help restore functional vision. The site also notes the implants may defer the need for a corneal transplant.

The segments are made of PMMA, come in different thicknesses, and are designed to be removable or replaceable. They are surgically inserted through a small radial incision at roughly two-thirds corneal depth.

What this means in practice

  • Who it may suit: people with keratoconus whose vision is no longer well corrected by glasses or contact lenses but who are not yet at the transplant stage. A candidate evaluation with a corneal specialist is the deciding step.
  • What it does not do: it does not cure keratoconus or halt the underlying disease process; the page describes it as reshaping and stabilizing the cornea to improve vision, not as a disease-modifying treatment.
  • Trade-off: it is a surgical procedure with the usual risks of corneal surgery, and because the segments are removable or exchangeable, adjustment is possible — a practical advantage over irreversible options.

A useful next step is to ask an ophthalmologist whether your corneal thickness, cone location and vision correction history make you a candidate, and how Intacs would compare with specialty contact lenses or cross-linking in your case.

Who is a good candidate for Intacs versus a corneal transplant?

A good candidate for Intacs is generally someone with keratoconus whose cornea is still stable enough for a device to reshape and support it, and who is looking to improve functional vision while postponing a transplant. The site describes Intacs as ophthalmic implants placed in the corneal stroma outside the central optical zone, inserted through a small radial incision at roughly two-thirds depth, and made in different thicknesses. It states they are designed to reduce or eliminate myopia and astigmatism in keratoconus patients so functional vision may be restored and a corneal transplant potentially deferred. The site also notes the implants are designed to allow removal or replacement.

A corneal transplant is the more invasive path, typically considered when the cornea is too thin, scarred, or otherwise unsuitable for an implant approach, or when vision cannot be adequately improved by other means. The site frames Intacs as an option to improve vision prior to considering a cornea transplant, which suggests candidacy depends on the individual cornea's shape, thickness and the degree of vision loss rather than on a single threshold.

Practical decision criteria

  • Corneal thickness and shape: Thin or irregular corneas may not support an implant safely; this is a clinical judgment.
  • Vision goals: Intacs aim to reshape and stabilize the cornea to improve functional vision; a transplant replaces damaged corneal tissue.
  • Reversibility: Intacs are designed to be removable or replaceable, which matters if the disease progresses or the result is unsatisfactory.
  • Staging: The site positions Intacs before transplant consideration, so candidacy is often about whether the cornea can still be helped by reshaping.

The next step is a corneal specialist evaluation with topography and thickness measurements, since the site does not specify candidacy thresholds. For broader context on keratoconus care, see American Optometric Association and National Eye Institute.

What happens during the Intacs insertion procedure and how long is recovery?

Intacs are small arc-shaped segments inserted into the cornea, not on its surface. According to the page, they are placed in the corneal stroma at roughly two-thirds depth, outside the central optical zone, through a small radial incision. The aim is to reshape and stabilize a keratoconic cornea so functional vision can improve and a transplant may potentially be deferred. The segments are made of PMMA and come in different thicknesses; the page also states they are designed to allow removal or replacement.

What the procedure involves

  • Placement: peripheral corneal stroma, about two-thirds depth, outside the central optical zone.
  • Access: a small radial incision in the stroma.
  • Effect: reshaping and stabilizing the cornea rather than replacing it.
  • Reversibility: the page says the segments are designed to be removed or replaced.

Recovery

The page does not give a recovery timeline, so treat any specific number of days or weeks as advice to confirm with the treating surgeon rather than a product detail. In practical terms, a patient considering this option should ask the clinic about:

  • Expected visual fluctuation in the first weeks and when vision typically stabilizes.
  • Restrictions on driving, screen work and strenuous activity.
  • Follow-up visit frequency and what signs warrant an urgent call.
  • Whether removal or exchange is covered if results are unsatisfactory.

A useful next step is to ask the surgeon how many Intacs procedures they perform, what outcomes they see in corneas similar to yours, and how they decide segment thickness. For broader context on keratoconus care, official sites such as American Academy of Ophthalmology and National Eye Institute explain the condition and treatment categories.

Can Intacs implants be removed or replaced later, and what are the risks?

Yes. According to the product page, Intacs® corneal implants are designed to allow removal or replacement. They sit in the corneal periphery at roughly two-thirds depth, outside the central optical zone, and are inserted through a small radial incision in the corneal stroma. That peripheral placement is what makes later removal or exchange feasible, and it is also why the segments are made in different thicknesses: the choice of thickness is part of tuning the effect on the cornea's shape.

What the page does and does not say about risks

The page describes the intended benefit—reshaping and stabilizing the cornea to reduce or eliminate myopia and astigmatism in keratoconus, with the aim of restoring functional vision and potentially deferring a corneal transplant. It does not list complications, contraindications, or success rates. Treat any specific risk figures as something to get from the treating surgeon, not from this site.

Practical risk categories to discuss with a surgeon

These are general considerations for intrastromal corneal segment surgery, not claims taken from the page:

  • Procedure-related: infection, incomplete or uneven channel creation, and perforation into the anterior chamber—rare but the most serious.
  • Implant-related: segment migration or extrusion, particularly if the cornea is very thin at the insertion site; visibility of the segment edge under the epithelium.
  • Vision-related: induced astigmatism or over- or under-correction, which is where thickness selection and possible exchange matter; glare or haloes in some patients.
  • Disease-related: keratoconus can continue to progress, so the improvement may not hold without separate treatment such as corneal cross-linking. Ask whether cross-linking is recommended before, during, or after implantation.

A concrete scenario

A patient with moderate keratoconus who is contact-lens intolerant and not yet ready for a transplant is the typical candidate profile implied by the page. For that person, the removable, exchangeable design is the main trade-off: it offers a reversible step before transplant, but reversibility does not make the surgery risk-free, and removal may not fully return the cornea to its prior state.

Next step

Ask the surgeon three questions: what is my corneal thickness at the planned insertion site, is cross-linking part of my plan, and what is your own rate of segment exchange or removal? For background on keratoconus management, the official patient resources at American Academy of Ophthalmology are a reasonable starting point.

How do Intacs compare with other keratoconus treatments like corneal cross-linking or contact lenses?

Intacs are a surgical option for keratoconus, and they work differently from cross-linking and specialty contact lenses rather than replacing them outright. The page describes Intacs as small PMMA segments inserted into the peripheral corneal stroma through a small radial incision, outside the central optical zone, to reshape and stabilize the cornea and reduce myopia and astigmatism. They are described as removable or replaceable and as potentially deferring a corneal transplant. The site presents them as the only FDA-approved intracorneal segments.

How the options differ in purpose

Option What it mainly does Typical role
Intacs Surgically reshapes the peripheral cornea to reduce prescription and stabilize shape A surgical step for suitable keratoconus patients, positioned by the site as an option before considering transplant
Corneal cross-linking Aims to strengthen the cornea and slow progression Disease-stabilizing treatment; general advice is that it is often discussed when progression is documented
Specialty contact lenses Correct vision optically over the irregular cornea Non-surgical vision correction, often the mainstay for irregular astigmatism

The key distinction is intent: cross-linking targets progression, contact lenses target vision correction, and Intacs target corneal shape and prescription. These are not mutually exclusive in practice; a patient might use lenses for daily vision and undergo cross-linking to limit worsening, with Intacs considered in selected cases.

Practical decision criteria

A reader with keratoconus should ask their eye care specialist three concrete questions: whether the cornea is actively progressing (which points toward stabilization strategies), whether glasses or specialty lenses provide acceptable functional vision, and whether the corneal thickness and shape make an intracorneal procedure appropriate. The page's own framing is that Intacs may improve vision "prior to considering a cornea transplant"—so it is best understood as one option along a spectrum, not a first-line substitute for lenses.

For broader context on keratoconus management, compare with American Academy of Ophthalmology and National Eye Institute.

Related questions

More questions →
What Is intacsforkeratoconus.com About?

intacsforkeratoconus.com is an informational site about Intacs® Corneal Implants, ophthalmic medical devices intended for people with keratoconus. It explains what the implants are, how they are positioned in the eye, and how they may reduce or eliminate myopia and astigmatism so functional vision can potentially be restored and a corneal transplant potentially deferred. The site is not an online store; it presents product and condition information and offers separate sections for patients and medical professionals.

What the site covers

The site centers on two connected topics: the Intacs® device and keratoconus itself.

Intacs® Corneal Implants

According to the site, Intacs® Corneal Implants are described as the only FDA-approved intracorneal segments. Key details presented include:

  • Purpose: Designed for the reduction or elimination of myopia and astigmatism in patients with keratoconus, so functional vision may be restored and the need for a corneal transplant can potentially be deferred.
  • Mechanism: When placed in the corneal stroma outside the central optical zone, the product reshapes and stabilizes the cornea.
  • Placement: The segments are designed to sit in the periphery of the cornea at approximately two-thirds depth and are surgically inserted through a small radial incision in the corneal stroma.
  • Material and sizing: Manufactured from polymethylmethacrylate (PMMA) and available in different thicknesses.
  • Reversibility: The implants are designed to allow removal or replacement.

Keratoconus

The site explains keratoconus as a disease that thins the cornea, causing it to progressively bulge into a cone-like shape. That change in shape can have a dramatic impact on vision. Intacs® is presented as a possible option to improve vision before considering a cornea transplant.

Who the site is for

The navigation includes sections for Patients, Medical Professionals, and Contact Us, suggesting the content is organized for two audiences: people researching keratoconus treatment options and clinicians seeking product information. The site also links to a privacy policy and legal notice and is published by Addition Technology Inc. (copyright 2022).

What it does not provide

The available site content does not list pricing, purchasing options, or a directory of providers. It is a product and condition explainer rather than a transactional or booking site. Anyone considering Intacs® would need to discuss suitability, risks, and next steps with an eye care professional; the site itself presents the device's intended use rather than individualized medical guidance.

In short, intacsforkeratoconus.com is a focused resource for understanding what Intacs® Corneal Implants are, how they are designed to work in keratoconus, and where patients and professionals fit into that picture.

What Is Keratoconus and How Does It Affect Vision?

Keratoconus is a disease in which the cornea thins and progressively bulges into a cone-like shape. Because the cornea is the eye's clear front surface and does much of the focusing, that change in shape can have a dramatic impact on vision. Intacs® Corneal Implants are an option that may improve vision before a cornea transplant is considered.

What Keratoconus Does to the Eye

The cornea normally holds a rounded, stable curve. In keratoconus, the tissue thins, and the weakened cornea gradually protrudes into a cone. The result is a cornea whose shape no longer focuses light cleanly, which is why vision changes can be significant rather than minor.

How the Changed Shape Affects Vision

The site describes the impact in general terms: the altered corneal shape "can have a dramatic impact on one's vision." It does not list specific symptoms or measurements, so the practical takeaway is that the problem is structural — the eye's focusing surface is being reshaped by the disease — and that vision is the function most directly affected.

Where Intacs® Fits in Treatment

Intacs® Corneal Implants are described as ophthalmic medical devices designed for the reduction or elimination of myopia and astigmatism in patients with keratoconus, so that functional vision may be restored and a corneal transplant can potentially be deferred. In other words, they are positioned as an option to improve vision before a cornea transplant is considered.

Key details from the manufacturer's description:

  • Placement: The segments are placed in the periphery of the cornea, outside the central optical zone, at approximately two-thirds depth, inserted surgically through a small radial incision in the corneal stroma.
  • Effect: Once in the corneal stroma, the product reshapes and stabilizes the cornea.
  • Material and sizing: Made from polymethylmethacrylate (PMMA) and available in different thicknesses.
  • Reversibility: The implants are designed to allow removal or replacement.
  • Regulatory status: Described as the only FDA-approved intracorneal segments.
Question What the source states
What is keratoconus? A disease that thins the cornea, causing it to progressively bulge into a cone-like shape
How does it affect vision? The change in corneal shape can have a dramatic impact on vision
What do Intacs® do? Reduce or eliminate myopia and astigmatism in keratoconus patients, potentially deferring a corneal transplant
Can they be removed? Yes — designed to allow removal or replacement

What This Means for a Decision

If you or someone you know has keratoconus, the relevant question is whether an option that reshapes and stabilizes the cornea — without removing tissue from the central optical zone — is appropriate before proceeding to transplant. The source presents Intacs® as exactly that earlier-stage option, but it does not discuss candidacy criteria, outcomes, risks, or cost. Those specifics, and whether Intacs® is suitable for a particular eye, are matters to confirm with an eye care professional; the manufacturer's site also provides separate sections for patients and medical professionals for further detail.

Is Intacs® an FDA-Approved Alternative to a Corneal Transplant for Keratoconus?

Intacs® Corneal Implants are described on intacsforkeratoconus.com as the only FDA-approved intracorneal segments, and they are intended to reduce or eliminate myopia and astigmatism in patients with keratoconus so that functional vision may be restored and a corneal transplant potentially deferred. They are not a replacement for a transplant in every case: the site positions them as an option to consider before a cornea transplant, and suitability must be confirmed with an eye care professional.

What Intacs® are and what they are designed to do

According to the site, Intacs® are ophthalmic medical devices made from polymethylmethacrylate (PMMA) and are available in different thicknesses. When placed in the corneal stroma outside the central optical zone, they are designed to reshape and stabilize the cornea.

The stated goals are to:

  • Reduce or eliminate myopia and astigmatism in patients with keratoconus
  • Restore functional vision
  • Potentially defer the need for a corneal transplant procedure

How they are inserted, and whether they can be removed

The site states that Intacs® segments are designed to be placed in the periphery of the cornea at approximately two-thirds depth and are surgically inserted through a small radial incision in the corneal stroma. The devices are also designed to allow removal or replacement.

Question What the site states
Where are they placed? Periphery of the cornea, about two-thirds depth, outside the central optical zone
How are they inserted? Surgically, through a small radial incision in the corneal stroma
Can they be removed? Yes — designed to allow removal or replacement
Material PMMA, available in different thicknesses

Keratoconus and why an implant is considered

Keratoconus is described as a disease that thins the cornea and causes it to progressively bulge into a cone-like shape. That change in shape can have a dramatic impact on vision. Intacs® are presented as a possible way to improve vision before considering a cornea transplant.

How to decide whether this path applies to you

The site does not publish patient selection criteria, candidacy requirements, or outcome data beyond the general description above. The practical next step is therefore a consultation with an eye care professional who can assess your cornea and tell you whether Intacs® is appropriate for your situation or whether a corneal transplant or another approach is more suitable.

For general background, the site's own framing is the clearest guide: Intacs® are intended to potentially defer — not universally replace — a corneal transplant.

What Are Intacs® Corneal Implants and How Do They Treat Keratoconus?

Intacs® Corneal Implants are small ophthalmic devices surgically placed inside the cornea to reduce or eliminate the nearsightedness (myopia) and astigmatism caused by keratoconus, with the goal of restoring functional vision and potentially deferring a corneal transplant. They are described on intacsforkeratoconus.com as the only FDA-approved intracorneal segments, made from polymethylmethacrylate (PMMA) and available in different thicknesses. They are an option for keratoconus patients whose vision is affected by the condition—not a cure for keratoconus itself.

What Keratoconus Does to the Cornea

Keratoconus is a disease that thins the cornea and causes it to progressively bulge into a cone-like shape. Because the cornea is the eye's clear front surface, this change in shape can dramatically distort vision. The site frames Intacs® as a way to improve vision before a cornea transplant is considered.

How Intacs® Work

The mechanism, as described on the site:

  • Placement: The segments are inserted into the corneal stroma—the middle layer of the cornea—through a small radial incision.
  • Location: They sit in the periphery of the cornea, outside the central optical zone, at approximately two-thirds depth.
  • Effect: Once in place, the product reshapes and stabilizes the cornea, which is what reduces or eliminates the myopia and astigmatism caused by keratoconus.
  • Reversibility: The implants are designed to allow removal or replacement.

A useful way to picture it: rather than removing or replacing the cornea, the segments act like small supports placed under the outer edge of a bulging surface, nudging the overall shape back toward something more regular while leaving the center of the eye's optics untouched.

What the Procedure Is and Is Not

Question What the site supports
Does it treat keratoconus itself? No—it is designed to reduce or eliminate myopia and astigmatism in keratoconus patients so functional vision may be restored
Can it replace a transplant? It may potentially defer the need for a corneal transplant; it is presented as an option to improve vision prior to considering a transplant
Is it approved? Described as the only FDA-approved intracorneal segments
Can it be undone? Yes—segments are designed to allow removal or replacement
What is it made of? PMMA, in multiple thicknesses

Who This Information Is For

This overview suits patients recently diagnosed with keratoconus, or their families, who want to understand what Intacs® are before a specialist consultation. The site separates content for Patients and Medical Professionals, so candidacy, expected outcomes, and risks are best confirmed with an eye care professional rather than from the website alone. The site does not publish pricing or eligibility criteria, so those questions belong in a consultation.

How Are Intacs® Corneal Implants Inserted, and Can They Be Removed?

Intacs® Corneal Implants are inserted surgically through a small radial incision in the corneal stroma, placed in the periphery of the cornea at approximately two-thirds depth, outside the central optical zone. Yes—they are designed to allow removal or replacement. The implants are made from polymethylmethacrylate (PMMA) and come in different thicknesses, so the specific device used is chosen before or during the procedure.

What the Procedure Involves

According to the manufacturer's description, the surgical steps center on placing the segments in the peripheral cornea rather than the center:

  • Incision: A small radial incision is made in the corneal stroma.
  • Placement: The Intacs® segments are inserted into the corneal stroma at roughly two-thirds depth.
  • Position: They sit in the periphery of the cornea, outside the patient's central optical zone.

Once in place, the product reshapes and stabilizes the cornea. The intended effect is to reduce or eliminate myopia and astigmatism in patients with keratoconus, so functional vision may be restored and a corneal transplant potentially deferred.

Why the Peripheral Position Matters

Because the segments are placed outside the central optical zone, the mechanism is a reshaping of the cornea's peripheral structure rather than a direct treatment of the center. This is the key difference from simply describing the device as a "lens"—it is an implant that changes corneal shape from the outside in.

Can They Be Removed or Replaced?

Yes. The manufacturer states the Intacs® are designed to allow removal or replacement. This matters for two practical reasons:

  1. Adjustability over time: If the outcome is not as intended, or the cornea changes, the option to remove or exchange the segments exists by design.
  2. Thickness selection: Since the implants are available in different thicknesses, replacement can involve a different segment thickness rather than only removal.

The website does not describe the removal procedure itself, recovery after removal, or how often replacement occurs. Those specifics would need to come from the treating surgeon.

Who This Is For

The device is described for patients with keratoconus—a disease that thins the cornea and causes it to progressively bulge into a cone-like shape, dramatically affecting vision. Intacs® are positioned as an option to improve vision before considering a cornea transplant. The site also states they are the only FDA-approved intracorneal segments.

Question Answer from the manufacturer's information
How are they inserted? Through a small radial incision in the corneal stroma
Where are they placed? Corneal periphery, about two-thirds depth, outside the central optical zone
What are they made of? Polymethylmethacrylate (PMMA)
Do they come in different sizes? Yes, different thicknesses
Can they be removed? Yes, designed to allow removal or replacement
What is the goal? Reduce or eliminate myopia and astigmatism in keratoconus; potentially defer corneal transplant

What to Confirm With a Surgeon

The website covers the device concept but not candidacy criteria, surgical risks, recovery timelines, or cost. Before deciding, ask the treating ophthalmologist to confirm:

  • Whether your corneal thickness and cone location make you a candidate for peripheral placement at two-thirds depth.
  • Which segment thickness they recommend and why.
  • What removal or replacement would involve in your case, and under what circumstances they would consider it.

The site itself offers patient, medical professional, and contact sections for further inquiries.

Website Overview

Identifiable technologies and additional version or configuration signals make the service easier to fingerprint, which may help targeted scanners narrow their checks. An established domain and managed infrastructure suggest continuity of operations and may support dependable delivery, although neither guarantees service quality.

Domain and Registration

Registered in 2004, this domain has about 22 years of history. That suggests continuity, although ownership and purpose may have changed. Transfer-protection status is present, helping reduce the risk of unauthorized domain transfers. The registrar is GoDaddy.com, LLC, a widely used domain service provider. The domain uses the common .com extension, which is not an independent safety signal.

DNS and Email

MX records exist, but SPF, DKIM and DMARC were not detected. Protection against domain impersonation may be incomplete. Nameservers are provided by GoDaddy, indicating managed DNS hosting. MX records point to the emailsrvr.com email service. No CNAME was found; the observed records resolve directly to addresses. DNSSEC signatures were not detected, so this additional DNS authenticity protection is not confirmed.

TLS and Certificates

The certificate uses an RSA 2048-bit public key, offering broad client compatibility. The server supplied a complete certificate chain. No organization name is present in the certificate; the available fields are consistent with domain validation. The certificate is valid for about 198 days in total, with 187 days remaining. The certificate covers the main domain and its usual www hostname.

HTTP and Browser Security

The Server header exposes the software version: DPS/2.0.0+sha-24a41f4. This makes version-targeted checks easier, but is not proof of an exploitable vulnerability. The response lacks these common security headers: X-Content-Type-Options, Referrer-Policy, Permissions-Policy. No X-Powered-By header was found, reducing one common source of backend fingerprinting information. No obvious internal addresses or debug information were found in the headers. Cookie security attributes are unknown.

Technology Stack Analysis

The public page identifies Starfield Technologies; Go Daddy Website Builder 8.0.0000, with exact versions exposed for 1 technologies. These details can narrow vulnerability checks, although exposure alone is not a vulnerability.

Search and Social Sharing

The Generator tag identifies Starfield Technologies; Go Daddy Website Builder 8.0.0000, making the publishing system easier to fingerprint. Twitter Card metadata is configured. The title has 38 characters, within a common display range. A meta description is present, with 153 characters. The observed directives allow indexing and link following.

Hosting and Email

DNSGoDaddy
HostingAmazon.com, Inc.
Emailemailsrvr.com
Approximate IP geolocation (inferred; a CDN or proxy may differ from the origin server) United States flagUnited States Inferred 13.248.243.5

Registration details

RDAP / WHOIS

RegistrarGoDaddy.com, LLC
Registered2004-07-01
Expires2027-07-01
Domain statusclient delete prohibited、client renew prohibited、client transfer prohibited、client update prohibited
Nameserversns71.domaincontrol.com、ns72.domaincontrol.com
DNSSECunsigned

DNS records

DNS

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MXintacsforkeratoconus.commx1.emailsrvr.com360010
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NSintacsforkeratoconus.comns71.domaincontrol.com3600—
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TLS and certificates

TLS / SSL

AssessmentNormal configuration
Supported protocolsTLSv1.2、TLSv1.3
Negotiated protocolTLSv1.3
Certificate subjectintacsforkeratoconus.com
IssuerGoDaddy.com
Valid until2027-04-22T20:51 · Remaining when checked: 187 days
Verification detailsCertificate trust: Passed · Hostname match: Passed

HTTP response headers

HTTP

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content-security-policyframe-ancestors 'self' godaddy.com *.godaddy.com dev-godaddy.com *.dev-godaddy.com test-godaddy.com *.test-godaddy.com
set-cookieRedacted

Identified technologies

Starfield Technologies; Go Daddy Website Builder 8.0.0000

Pages, Search and Sharing

Meta descriptionIntacs® Corneal Implants are ophthalmic medical devices designed for patients with keratoconus, reducing or postponing the needs for a corneal transplant
Canonical URLhttps://intacsforkeratoconus.com/
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