EndoSerter®-PL
Experience DSEK Redefined.
Introducing the revolutionary EndoSerter®-PL. This exclusive, FDA approved, single-use graft insertion device is pre‑loaded with expertly processed Nano‑Thin™ or Ultra-Thin DSEK tissue.
Schedule a ConsultationDetails & Specifications
Schedule Your In-Service
Discuss with your Surgical Product Specialist today to schedule your in-service consultation and experience DSEK Redefined.
Instructional Video:
The EndoSerter-PL is an FDA approved, single-use graft insertion device pre‑loaded with expertly processed Nano‑Thin™ or Ultra-Thin DSEK tissue. The following video provides a detailed overview of how the EndoSerter-PL works, along with step-by-step instructions on using the EndoSerter-PL. Please take a moment to watch the video and then give our office a call to schedule an in-service: (844) 526-7632
Instructional Video
Product Info
This new and exclusive FDA approved, single-use graft insertion device is pre‑loaded with expertly processed Nano‑Thin™ or Ultra-Thin DSEK tissue.
DSEK REDEFINED
- Designed to allow consistent allograft positioning
- Simplifies the procedure, maximizing O.R. efficiency
- Reduces endothelium manipulation in the O.R.
More Information
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Educational Resources
Innovations in Corneal Endothelial Transplantation
Edward Holland, M.D. presents his experience of working with CorneaGen's...
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The Eye Bank Difference
Watch Dr. Matt Giegengack as he presents an informative educational...
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Using the EndoSerter® to Insert Nano-Thin™, the Thinnest DSEK Tissue
CorneaGen invites you to view Dr. Zaina Al-Mohtaseb’s 2019 AAO...
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EndoSerter® for DSEK
Watch Dr. Julie Schallhorn as she demonstrates her surgical techniques...
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How Thin is Nano-Thin? Discover the Thinnest DSAEK Yet.
Watch this free educational webinar as Dr. Edward J. Holland...
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Reimbursement
If you need assistance with reimbursement of corneal tissue, CorneaGen is pleased to provide its customers with reimbursement and medical claims assistance to help guide you in billing corneal tissue to your local Medicare carrier and other commercial insurance carriers.
Adverse Reaction Reporting
If you have had any complications occur in your recipients, we ask you please file a report with us so that we may comply with EBAA and FDA regulations.
Regulatory Information
CorneaGen’s labs maintain the highest levels of quality through review by the U.S. Food and Drug Administration. For more information, please contact our Quality Assurance and Regulatory Affairs Department at (877) 682-8502.