Bonwrx L T D

FDA Filings

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.

FDA Registration(s)
Registration Number3004099322
FEI Number3004099322
NameBONWRx Ltd
Owner & OperatorBONWRx Ltd
Contact Address924 TERMINAL RD
Lansing MI 48906 US
Official Correspondent
  • Ralph W Carmichael
  • x-917-6670623-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address924 TERMINAL RD
Lansing, MI 48906 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
BONWRx Ltd
VK1002020-02-03
BONWRx Ltd
VK Percutaneous Vertebral Augmentation System2020-02-03
BONWRx Ltd
VK100 Percutaneous Vertebral Augmentation System2019-11-08

Related Finance Registrations
NCAGE Code7MV89BONWRX LTD
CAGE Code7MV89BONWRX LTD
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