# Koros USA, Inc.

- Location (FDA's records): Moorepark, CA
- FDA decisions: 4 (2007–2013): 4 510(k) clearances
- Product codes: GZT (1), PDQ (1), HRS (1), LXH (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K120590: Dilator Tube Set (May 7, 2013)
- K101609: Self Retaining Soft Tissue Retractor (Dec 9, 2010)
- K082399: Pectus Strut (Nov 5, 2009)
- K071338: Flex Arm Retractor System (May 29, 2007)

Source page: https://510kreport.com/company/koros-usa