# Bio2 Technologies, Inc.

- Location (FDA's records): Woburn, MA
- FDA decisions: 3 (2014–2016): 3 510(k) clearances
- Product codes: MQV (2), HTY (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (1 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
- Novabone Products, LLC: 1 (https://510kreport.com/company/novabone-products)
- Inion, Ltd.: 1 (https://510kreport.com/company/inion)
- Osteobiologics, Inc.: 1 (https://510kreport.com/company/osteobiologics)
- Synthes: 1 (https://510kreport.com/company/synthes)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Xtremi-T, LLC: 1 (https://510kreport.com/company/xtremi-t)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Its most-cited devices
- K142463: Bio2 CLM BG Bioactive Scaffold (2014), cited by 1

## Recent decisions
- K152589: Bio2 CLM BG Bioactive Scaffold (Jan 12, 2016)
- K151876: Bio2 Fusion Implant System (Dec 30, 2015)
- K142463: Bio2 CLM BG Bioactive Scaffold (Dec 18, 2014)

Source page: https://510kreport.com/company/bio2-technologies