Cymedica Orthopedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CyMedica e-vive™ System; CY-1000 Ref K163067
Regimes: 510(k) Registry: 510(k)Motive Knee Wrap Ref K220738
Regimes: 510(k) Registry: 510(k)Motive™ Electrode Ref K230533
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Intellihab System Ref K210604
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cymedica Orthopedics, Inc. have in the registry?
The registry currently lists 5 devices for Cymedica Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cymedica Orthopedics, Inc.'s devices?
Among its 5 most recently registered devices, Cymedica Orthopedics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Cymedica Orthopedics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cymedica Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cymedica Orthopedics, Inc. in the registry?
The most recently registered devices listed for Cymedica Orthopedics, Inc. include CyMedica e-vive™ System; CY-1000, Motive Knee Wrap, Motive™ Electrode and QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator.