# Refractec, Inc.

- Location (FDA's records): Laguna Hills, CA
- FDA decisions: 3 (1998–2006): 2 510(k) clearances and 1 original PMA approval
- Product codes: HQR (1), HMR (1), MWD (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
- K053475: Optipoint Corneal Marker, Model VPT-Opt-450 (Mar 3, 2006)
- P010018: Viewpoint (TM) CK System (Apr 11, 2002)
- K980522: Refractec MCS-100 (Jul 22, 1998)

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