# Suretek Medical

- Location (FDA's records): Greenville, SC
- FDA decisions: 4 (2006–2006): 4 510(k) clearances
- Product codes: NUJ (3), JOW (1)
- Predicates its devices cite: 27 (0 its own); citations of its devices by later devices: 0 (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
- Vanguard Medical Concepts, Inc.: 3 (https://510kreport.com/company/vanguard-medical-concepts)
- Linvatec Corp.: 2 (https://510kreport.com/company/linvatec)
- Arthrocare Corp.: 2 (https://510kreport.com/company/arthrocare)
- Valleylab, Inc.: 2 (https://510kreport.com/company/valleylab)
- Huntleigh Healthcare, Inc.: 2 (https://510kreport.com/company/huntleigh-healthcare)
- Aircast, Inc.: 2 (https://510kreport.com/company/aircast)
- Smith & Nephew Dyonics, Inc.: 1 (https://510kreport.com/company/smith-nephew-dyonics)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)

## Recent decisions
- K052691: Suretek Medical Reprocessed Compression Sleeves (May 17, 2006)
- K052690: Suretek Reprocessed Laparoscopic Instruments (May 12, 2006)
- K052695: Suretek Medical Reprocessed Arthroscopic Blades and Burs (May 10, 2006)
- K052692: Suretek Medical Reprocessed Electrosurgical Electrodes (May 10, 2006)

Source page: https://510kreport.com/company/suretek-medical