# Thera Kinetics, Inc.

- Location (FDA's records): Mt. Laurel, NJ
- FDA decisions: 3 (1990–1991): 3 510(k) clearances
- Product codes: BXB (3)
- 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
- K912537: Jace Model K200 Knee CPM Device, Modification (Aug 16, 1991)
- K913227: Jace Model T300 Toe CPM Device (Aug 16, 1991)
- K903467: Jace Model 100 Knee CPM Device (Aug 10, 1990)

Source page: https://510kreport.com/company/thera-kinetics