This page includes the latest FDA filings for Arbor Vita Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3008361618 |
| FEI Number | 3008361618 |
| Name | ARBOR VITA CORPORATION |
| Owner & Operator | Arbor Vita Corporation |
| Contact Address | 48371 Fremont Blvd., Suite 101 Fremont CA 94538 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 48371 Fremont Blvd Ste 101 Fremont, CA 94538 US |
| Establishment Type | Manufacture Device in the United States for Export Only |
Device Company | Device | Date |
|---|---|---|
ARBOR VITA CORPORATION | OncoE6? Cervical Test | 2017-08-30 |
| NCAGE Code | 1WBJ2 | ARBOR VITA CORPORATION |
| CAGE Code | 1WBJ2 | ARBOR VITA CORPORATION |
| S.A.M. Registration | 1WBJ2 [37387904] | ARBOR VITA CORPORATION |
| S.A.M. Registration | 1WBJ2 [37387904] | ARBOR VITA CORPORATION |
| SEC | 0001063008 | ARBOR VITA CORP |