# Medical Device Services

- Location (FDA's records): St. George, UT
- FDA decisions: 6 (2002–2002): 6 510(k) clearances
- Names in FDA's records: Medical Device Services (5); Medical Device Services, Inc. (1)
- Product codes: JOW (2), HWE (1), HET (1), KGE (1), KAB (1)
- Predicates its devices cite: 3 (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
- Smith & Nephew Dyonics, Inc.: 1 (https://510kreport.com/company/smith-nephew-dyonics)
- Symbiosis Corp.: 1 (https://510kreport.com/company/symbiosis)
- The Kendal Co.: 1 (https://510kreport.com/company/kendal)

## Recent decisions
- K022753: Reprocesses Used Disposable Sequential Compression Sleeves/Wraps (Nov 14, 2002)
- K022751: Reprocessed Used Disposable Hot and Cold Biopsy Forceps (Nov 4, 2002)
- K022748: Reprocssed Used Disposable Endoscopic Scissors and Graspers (Oct 9, 2002)
- K022743: Reprocessed Disposable Trocars (Oct 9, 2002)
- K022744: Reprocessed Used Disposable Arthroscopic Blades and Burs (Sep 18, 2002)
- K012979: Compressible Limb Sleeve (May 8, 2002)

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