# Osseon Therapeutics, Inc.

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: NDN (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 2 (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.: 4 (https://510kreport.com/company/kyphon)
- Care Fusion: 2 (https://510kreport.com/company/care-fusion)
- Cardinal Health, Inc.: 1 (https://510kreport.com/company/cardinal-health)

## Firms that cite its devices most
- Osseon, LLC: 2 (https://510kreport.com/company/osseon)

## Its most-cited devices
- K122533: Osseoflex SB Inflatable Bone Tamp (2012), cited by 2

## Recent decisions
- K122533: Osseoflex SB Inflatable Bone Tamp (Oct 23, 2012)

Source page: https://510kreport.com/company/osseon-therapeutics