# Jace Systems, Inc.

- Location (FDA's records): Moorestown, NJ
- FDA decisions: 6 (1992–1994): 6 510(k) clearances
- Product codes: BXB (3), JFA (2), IPF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Empi: 1 (https://510kreport.com/company/empi)
- Vision Quest Industries, Inc.: 1 (https://510kreport.com/company/vision-quest-industries)

## Its most-cited devices
- K931781: Jace Tri-Stim Device (1993), cited by 2

## Recent decisions
- K933059: Artromot-E, Elbow / Artromot-S, Shoulder CMP Mod. (Jun 22, 1994)
- K931016: Jace Model H440 Hand CPM Device (Jun 22, 1994)
- K931781: Jace Tri-Stim Device (Oct 8, 1993)
- K922185: Jace Knee Extension System -- Modification (Jun 11, 1992)
- K921351: Jace Model PM-410 Hand CPM Device (May 4, 1992)
- K920380: Jace Model W550 Wrist CPM Device (Feb 11, 1992)

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