Bonwrx, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bonwrx, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VK100 Percutaneous Vertebral Augmentation System
1
Total
1
Cleared
0
Denied
Bonwrx, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Lansing, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bonwrx, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bonwrx, Ltd.
1 devices