This page includes the latest FDA filings for First Use L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3005370013 |
| FEI Number | 3005370013 |
| Name | FIRST USE LLC |
| Owner & Operator | FIRST USE LLC |
| Contact Address | 709 RAINWATER DR. -- Lexington KY 40515 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2500 SANDERSVILLE RD. LEXINGTON, KY 40511 US |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
FIRST USE LLC | GAYHEART CORNEAL TREPHINE | 2005-09-13 |