This page includes the latest FDA filings for Lia Diagnostics Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3015042202 |
| FEI Number | 3015042202 |
| Name | Lia Diagnostics Production Facility |
| Owner & Operator | Lia Diagnostics, Inc. |
| Contact Address | 1015 Chestnut Street Philadelphia PA 19107 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 3401 Grays Ferry Ave, Building 176 Room 121 Philadelphia, PA 19146 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
| Lia Diagnostics, Inc. | Lia Pregnancy Test | 2021-03-23 |
| Lia Diagnostics, Inc. | Lia Pregnancy Test | 2021-03-23 |
Lia Diagnostics Production Facility [Lia Diagnostics, Inc.] | Lia | 2018-11-20 |
Lia Diagnostics Production Facility [Lia Diagnostics, Inc.] | Lia Pregnancy Test | 2018-11-20 |
| NCAGE Code | 7MXA7 | LIA DIAGNOSTICS, INC.!DBA LIA DIAGNOSTICS |
| CAGE Code | 7MXA7 | LIA DIAGNOSTICS, INC. LIA DIAGNOSTICS |
| SEC | 0001656738 | LIA Diagnostics Inc. of DELAWARE |