Joint Mobilizer Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Joint Mobilizer Systems, Inc. makes
Joint Mobilizer Systems, Inc. manufactures mechanical mobilizers designed to assist in the passive range-of-motion therapy for joints, including ankle and knee-to-hip systems. These devices are intended for clinical and home use to improve joint flexibility and mobility. The products are engineered to apply controlled force to facilitate rehabilitation and recovery. They are primarily used in physical therapy settings and patient self-care programs.
The company’s portfolio consists of Class I medical devices, which are generally considered low-risk. These devices are subject to 510(k) clearance through the FDA’s regulatory pathway. The products are listed under the FDA’s 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Ankle Mobilizer Ref K842882
Regimes: 510(k) Registry: 510(k)Knee-Hip Mobilizer Ref K842881
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Joint Mobilizer Systems, Inc. have in the registry?
The registry currently lists 2 devices for Joint Mobilizer Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Joint Mobilizer Systems, Inc.'s devices?
Among its 2 most recently registered devices, Joint Mobilizer Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Joint Mobilizer Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Joint Mobilizer Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Joint Mobilizer Systems, Inc. in the registry?
The most recently registered devices listed for Joint Mobilizer Systems, Inc. include ANKLE MOBILIZER and KNEE-HIP MOBILIZER.