This page includes the latest FDA filings for Entrepix Medical L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010115803 |
| FEI Number | 3010115803 |
| Name | ENTREPIX MEDICAL LLC |
| Owner & Operator | Entrepix Medical LLC |
| Contact Address | 4717 E. Hilton Ave Suite 200 Phoenix AZ 85034 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 4717 E. Hilton Ave Suite 200 Phoenix, AZ 85034 US |
| Establishment Type | Remanufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
| ENTREPIX MEDICAL, LLC | Planatome® | 2020-10-09 |
| ENTREPIX MEDICAL, LLC | Planatome® | 2020-10-09 |
| ENTREPIX MEDICAL, LLC | Planatome® | 2020-10-09 |
| ENTREPIX MEDICAL, LLC | Planatome® | 2020-10-09 |
ENTREPIX MEDICAL LLC | Planatome | 2017-12-21 |