Corneagen

FDA Filings

This page includes the latest FDA filings for Corneagen. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3005357288
• FEI Number: 3005357288
• Name: CorneaGen, Inc.
• Owner & Operator: CorneaGen
• Contact Address: 101 N Chestnut St Suite 303; Winston Salem NC 27101 US
• Official Correspondent:
  • Scott Carlisle
  • x-336-5169600-x
• Registration Status: 1
• Initial Importer: Y
• Registration Expiration: 2020-04-25
• Registration Address: 101 N Chestnut St Ste 303 ; Winston Salem, NC 27101 US
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
PMN P120023 | LQE CorneaGen, Inc. [CorneaGen]	KAMRA Inlay	2018-04-27
PMA P120023S005 CorneaGen	KAMRA INLAY	2017-07-18
PMA P120023S004 CorneaGen	KAMRA INLAY	2017-05-16
PMA P120023S002 CorneaGen	KAMRA INLAY	2016-10-07
PMA P120023S001 CorneaGen	KAMRA INLAY	2016-05-12
PMA P120023 CorneaGen	KAMRA INLAY	2015-04-17

Similar & Related FDA Registered Companies

• CorneaGen, Inc
• CorneaGen LLC