This page includes the latest FDA filings for Vertos Medical Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3006450448 |
| FEI Number | 3006450448 |
| Name | Vertos Medical Inc. |
| Owner & Operator | Vertos Medical Inc. |
| Contact Address | 95 Enterprise Suite 325 Aliso Viejo CA 92656 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 95 Enterprise Ste 325 Aliso Viejo, CA 92656 US |
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
| VERTOS MEDICAL, INC. | mild Device Kit MDK-0001 | 2024-12-02 |
| VERTOS MEDICAL, INC. | mild Device Kit | 2024-12-02 |
| VERTOS MEDICAL, INC. | mild Device Kit MDK-0001 | 2018-03-29 |
Vertos Medical Inc. | mild Device Kit | 2010-05-21 |
| NCAGE Code | 51UD2 | VERTOS MEDICAL, INC. |
| CAGE Code | 51UD2 | VERTOS MEDICAL, INC. |
| S.A.M. Registration | 51UD2 [11925561] | VERTOS MEDICAL, INC. |
| SEC | 0001327078 | VERTOS MEDICAL INC of DELAWARE |