FDA.reportPublic FDA data

BONWRx Ltd

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30040993223004099322BONWRx Ltd1N2026-01-01924 TERMINAL RD Lansing MI US 48906

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
218711804004386K192403VK100 Percutaneous Vertebral Augmentation SystemNDN2019-11-08

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NDN22019-11-08

PMN#