# Medmetric Corp.

- Location (FDA's records): San Diego, CA
- FDA decisions: 8 (1980–1995): 8 510(k) clearances
- Product codes: LYH (3), FTY (1), LXI (1), ISD (1), FWZ (1), IKK (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
- K943197: KT1000/S Knee Ligament Arthrometer (Mar 2, 1995)
- K942059: KT2000 Knee Ligament Arthrometer (Sep 20, 1994)
- K904823: Flexercycle (Jan 30, 1991)
- K904898: Torque Frame QTF1000 (Nov 28, 1990)
- K854254: Tension-Isometer (Nov 15, 1985)
- K812806: KT-1000 Device (Nov 10, 1981)
- K812713: Drawer Test (Nov 5, 1981)
- K801572: Surg-Assist (Aug 4, 1980)

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