This page includes the latest FDA filings for Hansen Ophthalmic Development Lab. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 1935505 |
| FEI Number | 1935505 |
| Name | HANSEN OPHTHALMIC DEVELOPMENT LAB |
| Owner & Operator | HANSEN OPHTHALMIC DEVELOPMENT LAB |
| Contact Address | 745 AVALON PL Coralville IA 52241 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 745 AVALON PL CORALVILLE, IA 52241 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
HANSEN OPHTHALMIC DEVELOPMENT LAB | Burian-Allen ERG Electrode | 2007-12-20 |
HANSEN OPHTHALMIC DEVELOPMENT LAB | OSSOINIG SCLERAL SHELLS | 1992-12-21 |
HANSEN OPHTHALMIC DEVELOPMENT LAB | TSE-ANDERSON MODIFIED LACRIMAL GROOV | 1984-05-09 |