# Greenleaf Medical Systems, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 4 (1989–1995): 4 510(k) clearances
- Product codes: KQX (2), LBB (2)
- 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
- K943929: Dataglove and Movement Analysis System (Mas) (May 15, 1995)
- K935757: Greenleaf Eval System/ Greenleaf Solosystem (Apr 15, 1994)
- K893537: Greenleaf Hand Impairment Evaluation System (Oct 10, 1989)
- K884723: (Dataglove) Hand Impairment Evaluation System (Feb 8, 1989)

Source page: https://510kreport.com/company/greenleaf-medical-systems