Jace Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Jace Systems, Inc. makes
Jace Systems, Inc. manufactures continuous passive motion (CPM) devices for the wrist, hand, elbow, and shoulder, as well as knee extension systems and electrical stimulation devices.
The company is based in the United States, and its portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Jace Model W550 Wrist Cpm Device Ref K920380
Regimes: 510(k) Registry: 510(k)Jace Model H440 Hand Cpm Device Ref K931016
Regimes: 510(k) Registry: 510(k)Jace Tri-Stim Device Ref K931781
Regimes: 510(k) Registry: 510(k)Jace Knee Extension System -- Modification Ref K922185
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Jace Model Pm-410 Hand Cpm Device Ref K921351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jace Systems, Inc. have in the registry?
The registry currently lists 6 devices for Jace Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jace Systems, Inc.'s devices?
Among its 6 most recently registered devices, Jace Systems, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Jace Systems, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Jace Systems, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jace Systems, Inc. in the registry?
The most recently registered devices listed for Jace Systems, Inc. include JACE MODEL W550 WRIST CPM DEVICE, JACE MODEL H440 HAND CPM DEVICE, JACE TRI-STIM DEVICE and JACE KNEE EXTENSION SYSTEM -- MODIFICATION.