# Arthocare Corporation

- Location (FDA's records): Austin, TX
- FDA decisions: 6 (2001–2016): 6 510(k) clearances
- Product codes: MBI (3), GAT (2), GEI (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrocare Corp.: 6 (https://510kreport.com/company/arthrocare)
- Opus Medical, Inc.: 2 (https://510kreport.com/company/opus-medical)

## Firms that cite its devices most
- Arthrocare Corp.: 2 (https://510kreport.com/company/arthrocare)
- Bovie Medical Corporation: 2 (https://510kreport.com/company/bovie-medical)
- Responsive Arthroscopy, LLC: 1 (https://510kreport.com/company/responsive-arthroscopy)

## Its most-cited devices
- K120791: Ambient Turboflash 90 Ifs (2012), cited by 2
- K131182: Multifix S Knotless Fixation Device (2013), cited by 2
- K121306: Smartstitch M-Connector Ultra Smartstitch Suture Device Handle Smartstitch Suture Device Handle (2012), cited by 1

## Recent decisions
- K153669: MultiFIX S Ultra Knotless Fixation System (Jan 19, 2016)
- K131182: Multifix S Knotless Fixation Device (Jul 29, 2013)
- K120791: Ambient Turboflash 90 Ifs (Dec 11, 2012)
- K123268: Smartstitch Perfectpasser System (Nov 7, 2012)
- K121306: Smartstitch M-Connector Ultra Smartstitch Suture Device Handle Smartstitch Suture Device Handle (Jul 12, 2012)
- K013334: Endoflip (Dec 13, 2001)

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