# Neosteo

- Location (FDA's records): Nantes, FR
- FDA decisions: 6 (2013–2022): 6 510(k) clearances
- Product codes: HWC (4), JDR (1), HRS (1)
- 510(k) review time since 2016: median 175 days, against 144 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 14 (2 its own); citations of its devices by later devices: 5 (2 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
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Newclip Technics: 2 (https://510kreport.com/company/newclip-technics)
- Extremity Medical, LLC: 1 (https://510kreport.com/company/extremity-medical)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Smt Schilling Metalltechnik GmbH: 1 (https://510kreport.com/company/smt-schilling-metalltechnik)
- Biopro, Inc.: 1 (https://510kreport.com/company/biopro)
- Memometal Technologies: 1 (https://510kreport.com/company/memometal-technologies)
- New Deal, S.A.: 1 (https://510kreport.com/company/new-deal)

## Firms that cite its devices most
- Extremity Medical, LLC: 2 (https://510kreport.com/company/extremity-medical)
- Lesspine Innovations: 1 (https://510kreport.com/company/lesspine-innovations)

## Its most-cited devices
- K131471: Self-Compressive Screw (2013), cited by 3
- K153182: Self- Compressive Screw (2015), cited by 1
- K150772: Snap-Off Self-Compressive Screw (2015), cited by 1

## Recent decisions
- K212545: FlexitSystem Knee osteotomy system (Feb 11, 2022)
- K192447: Superelastic Staple (Feb 28, 2020)
- K191424: Interphalangeal Joint Fusion Device Range (Aug 28, 2019)
- K153182: Self- Compressive Screw (Nov 25, 2015)
- K150772: Snap-Off Self-Compressive Screw (May 8, 2015)
- K131471: Self-Compressive Screw (Aug 28, 2013)

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