# Osseofuse, Inc.

- Location (FDA's records): Fullerton, CA
- FDA decisions: 2 (2013–2014): 2 510(k) clearances
- Product codes: DZE (2)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 1 (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
- Dynamic Innovations, Inc.: 2 (https://510kreport.com/company/dynamic-innovations)
- Osstem Implant Co., Ltd.: 1 (https://510kreport.com/company/osstem-implant)
- Neobiotech Co., Ltd.: 1 (https://510kreport.com/company/neobiotech)
- Implant Direct, LLC: 1 (https://510kreport.com/company/implant-direct)
- Nobel Biocare Uas, Inc.: 1 (https://510kreport.com/company/nobel-biocare-uas)
- Lifecore Biomedical, Inc.: 1 (https://510kreport.com/company/lifecore-biomedical)

## Firms that cite its devices most
- Kj Meditech Co., Ltd.: 1 (https://510kreport.com/company/kj-meditech)

## Its most-cited devices
- K133050: One Plus Implant System (2014), cited by 1

## Recent decisions
- K133050: One Plus Implant System (Sep 19, 2014)
- K131748: Osseofuse Dental Implant System (Oct 31, 2013)

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