# Surx, Inc.

- Location (FDA's records): Livermore, CA
- FDA decisions: 3 (2002–2002): 3 510(k) clearances
- Product codes: MUK (3)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 4 (3 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
- Vidamed, Inc.: 3 (https://510kreport.com/company/vidamed)
- Arthrocare Corp.: 2 (https://510kreport.com/company/arthrocare)
- Oratec Interventions, Inc.: 2 (https://510kreport.com/company/oratec-interventions)
- Louisville Laboratories, Inc.: 1 (https://510kreport.com/company/louisville-laboratories)
- Empi: 1 (https://510kreport.com/company/empi)

## Firms that cite its devices most
- Novasys Medical, Inc.: 1 (https://510kreport.com/company/novasys-medical)

## Its most-cited devices
- K011190: Surx Radiofrequency Electrosurgical Generator System and Accessories (Surx LP System) (2002), cited by 2
- K020952: Surx RF System (2002), cited by 1
- K020126: Modification to Surx Radiofrequency Electrosurgical Generator System and Accessories (Surx TV System) (2002), cited by 1

## Recent decisions
- K020952: Surx RF System (May 30, 2002)
- K020126: Modification to Surx Radiofrequency Electrosurgical Generator System and Accessories (Surx TV System) (Mar 15, 2002)
- K011190: Surx Radiofrequency Electrosurgical Generator System and Accessories (Surx LP System) (Jan 8, 2002)

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