# Fxdevices

- Location (FDA's records): Boca Raton, FL
- FDA decisions: 4 (2007–2010): 4 510(k) clearances
- Product codes: HWC (3), KCT (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 5 (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
- Triage Medical, Inc.: 1 (https://510kreport.com/company/triage-medical)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Symmetry Medical USA, Inc.: 1 (https://510kreport.com/company/symmetry-medical-usa)

## Firms that cite its devices most
- Smith & Nephew, Inc.: 2 (https://510kreport.com/company/smith-nephew)
- Pega Medical, Inc.: 2 (https://510kreport.com/company/pega-medical)

## Its most-cited devices
- K080649: Pogo Screw (2008), cited by 4
- K092189: Pogo Screw (2009), cited by 1

## Recent decisions
- K091806: Pogo Screw Instrumentation Tray (Feb 22, 2010)
- K092189: Pogo Screw (Sep 18, 2009)
- K080649: Pogo Screw (Nov 25, 2008)
- K070393: Lagwire System (May 4, 2007)

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