# Bonwrx, Ltd.

- Location (FDA's records): Lansing, MI
- FDA decisions: 1 (2019–2019): 1 510(k) clearance
- Product codes: NDN (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kyphon, Inc.: 1 (https://510kreport.com/company/kyphon)

## Recent decisions
- K192403: VK100 Percutaneous Vertebral Augmentation System (Nov 8, 2019)

Source page: https://510kreport.com/company/bonwrx