# Clearmedical, Inc.

- Location (FDA's records): Bellevue, WA
- FDA decisions: 14 (2002–2005): 14 510(k) clearances
- Product codes: JOW (5), NLF (3), DXQ (1), NLL (1), GEI (1), NMJ (1), KBG (1), NLU (1)
- Predicates its devices cite: 7 (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
- Ethicon Endo-Surgery, Inc.: 4 (https://510kreport.com/company/ethicon-endo-surgery)
- ETHICON, Inc.: 2 (https://510kreport.com/company/ethicon)
- Symbiosis Corp.: 1 (https://510kreport.com/company/symbiosis)

## Recent decisions
- K033578: Reprocessed Reloadable Cutters, Staplers, and Appliers (Jul 11, 2005)
- K033579: Reprocessed Multiple Clip Appliers (Jul 11, 2005)
- K033591: Reprocessed Trocars (Jun 3, 2005)
- K033592: Reprocessed Surgical Scissors and Graspers (Jul 27, 2004)
- K033593: Reprocessed Single Use Devices Biopsy Forceps (Nov 20, 2003)
- K031416: Clearmedical/Critikon Blood Pressure Cuff; Clearmedical/Welch Allyn Blood Pressure Cuff (Jul 15, 2003)
- K012609: Clearmedical/Nellcor Oxisensor II, Neonatal/Adult, Model N-25 (Jul 3, 2002)
- K012622: Clearmedical/Nellcor Oxisensor II, Pediatric, Model D-20 (Jul 3, 2002)

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