# Internal Fixation Systems, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 4 (2006–2011): 4 510(k) clearances
- Product codes: HWC (3), HRS (1)
- Predicates its devices cite: 26 (0 its own); citations of its devices by later devices: 9 (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
- Synthes (Usa): 7 (https://510kreport.com/company/synthes-usa)
- Nexa Orthopedics, Inc.: 3 (https://510kreport.com/company/nexa-orthopedics)
- DePuy Orthopaedics, Inc.: 2 (https://510kreport.com/company/depuy-orthopaedics)
- Osteomed LP: 2 (https://510kreport.com/company/osteomed)
- Vilex, LLC: 2 (https://510kreport.com/company/vilex)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Gpc Medical Limited: 1 (https://510kreport.com/company/gpc-medical)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)

## Firms that cite its devices most
- Impact Medical, LLC: 3 (https://510kreport.com/company/impact-medical)
- Laura Cattabriga: 3 (https://510kreport.com/company/laura-cattabriga)
- Gold Standard Orthopaedics, LLC: 1 (https://510kreport.com/company/gold-standard-orthopaedics)
- Fx Solutions: 1 (https://510kreport.com/company/fx-solutions)
- Orthonovis, Inc.: 1 (https://510kreport.com/company/orthonovis)

## Its most-cited devices
- K110086: Ifs Profile Plates, Screws, and Washers (2011), cited by 4
- K061620: Ifs Cannulated Bone Screw (2006), cited by 3
- K071035: Ifs Bone Fixation Devices (2007), cited by 2

## Recent decisions
- K113399: Ifs Subtalar Implant (Dec 20, 2011)
- K110086: Ifs Profile Plates, Screws, and Washers (Sep 9, 2011)
- K071035: Ifs Bone Fixation Devices (Aug 13, 2007)
- K061620: Ifs Cannulated Bone Screw (Jul 26, 2006)

Source page: https://510kreport.com/company/internal-fixation-systems