Mid-America Medical Innovations, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Mid-America Medical Innovations, LLC makes
Mid-America Medical Innovations, LLC manufactures the CP Relief Wand and CP Relief Wand-OTC, devices designed for pain relief and management of chronic pelvic pain.
These Class II devices are listed under the FDA’s 510(k) pathway and are regulated in the United States.
Catalogue
Cp Relief Wand Ref K133779
Regimes: 510(k) Registry: 510(k)CP Relief Wand-OTC Ref K162630
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mid-America Medical Innovations, LLC have in the registry?
The registry currently lists 2 devices for Mid-America Medical Innovations, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mid-America Medical Innovations, LLC's devices?
Among its 2 most recently registered devices, Mid-America Medical Innovations, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Mid-America Medical Innovations, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mid-America Medical Innovations, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mid-America Medical Innovations, LLC in the registry?
The most recently registered devices listed for Mid-America Medical Innovations, LLC include CP RELIEF WAND and CP Relief Wand-OTC.