This page includes the latest FDA filings for Bonwrx L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3004099322 |
FEI Number | 3004099322 |
Name | BONWRx Ltd |
Owner & Operator | BONWRx Ltd |
Contact Address | 924 TERMINAL RD Lansing MI 48906 US |
Official Correspondent |
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Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 924 TERMINAL RD Lansing, MI 48906 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
BONWRx Ltd | VK100 | 2020-02-03 |
BONWRx Ltd | VK Percutaneous Vertebral Augmentation System | 2020-02-03 |
BONWRx Ltd | VK100 Percutaneous Vertebral Augmentation System | 2019-11-08 |
NCAGE Code | 7MV89 | BONWRX LTD |
CAGE Code | 7MV89 | BONWRX LTD |