This page includes the latest FDA filings for Corneagen Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| 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 |
|
| 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 |
Device Company | Device | Date |
|---|---|---|
| CORNEAGEN INC. | EndoSerter-PL | 2023-06-19 |
CorneaGen, Inc | EndoSerter-PL | 2022-02-02 |
CorneaGen, Inc. [CorneaGen] | KAMRA Inlay | 2018-04-27 |
| NCAGE Code | 7RC65 | CORNEAGEN INC.!DBA SIGHTLIFE SURGICAL |
| CAGE Code | 7RC65 | CORNEAGEN INC. SIGHTLIFE SURGICAL |
| S.A.M. Registration | 7RC65 [80420749] | CORNEAGEN INC. SIGHTLIFE SURGICAL |
| SEC | 0001687524 | CorneaGen Inc. of DELAWARE |