This page includes the latest FDA filings for Omnyx L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3008491142 |
| FEI Number | 3008491142 |
| Name | Omnyx, LLC |
| Owner & Operator | Omnyx |
| Contact Address | 1251 Waterfront Place Pittsburgh PA 15222 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 1251 Waterfront Place Pittsburgh, PA 15222 US |
| Establishment Type | Manufacture Device in the United States for Export Only |
Device Company | Device | Date |
|---|---|---|
| OMNYX, LLC | Dynamyx Digital Pathology Software | 2022-04-29 |
OMNYX, LLC | OMNYX IDP FOR HER2 MANUAL APPLICATION | 2014-04-01 |
Omnyx, LLC [Omnyx] | Dynamyx Digital Pathology Software | 2013-02-17 |