This page includes the latest FDA filings for Nextphase Medical Devices. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3007199740 |
| FEI Number | 3007199740 |
| Name | NextPhase Medical Devices |
| Owner & Operator | NextPhase Medical Devices |
| Contact Address | 150 Hopper Ave Waldwick NJ 07463 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 150 Hopper Ave Waldwick, NJ 07463 US |
| Establishment Type |
|
Device Company | Device | Date |
|---|---|---|
NextPhase Medical Devices | Brain injury adjunctive interpretive oculomotor assessment aid | 2019-02-25 |
NextPhase Medical Devices | Meditron Endolav EL-100 | 2010-10-20 |