This page includes the latest FDA filings for Micropore Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3009133183 |
| FEI Number | 3009133183 |
| Name | MICROPORE INC |
| Owner & Operator | Micropore Inc |
| Contact Address | 1000 Konica Drive Elkton MD 21921 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 1000 Konica Dr Elkton, MD 21921 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
| Micropore, Inc. | SpiraLith Ca | 2024-06-06 |
| Micropore, Inc. | SpiraLith Ca | 2022-10-03 |
| Micropore, Inc. | SpiraLith Ca | 2022-10-03 |
MICROPORE INC | SpiraLith Ca | 2011-06-17 |
| NCAGE Code | 1STE2 | MICROPORE, INC. |
| NCAGE Code | 78842 | MICROPORE INC |
| CAGE Code | 1STE2 | MICROPORE, INC. |
| CAGE Code | 78842 | MICROPORE INC |
| S.A.M. Registration | 1STE2 [42903703] | MICROPORE, INC. |
| SEC | 0001098483 | MICROPORE INC of DELAWARE |