# Retrax

- Location (FDA's records): Wausau, WI
- FDA decisions: 2 (1990–1993): 2 510(k) clearances
- Names in FDA's records: Retrax (1); Retrax, Inc. (1)
- Product codes: FHQ (1), FMF (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
- K920706: Magnetic Point Guard for Surgical Needles (May 26, 1993)
- K901508: Retrax Safety Syringe (Jun 14, 1990)

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