Prospera Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Prospera Corporation makes
Prospera Corporation manufactures transcutaneous electrical nerve stimulation (TENS) devices designed for over-the-counter (OTC) use, including electronic pulse massagers with TENS functionality. These devices are intended for pain relief and muscle relaxation through low-voltage electrical stimulation.
The company’s TENS devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) database, and the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Prospera Otc Tens Electronic Pulse Massager Ref K122744
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prospera Corporation have in the registry?
The registry currently lists 2 devices for Prospera Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prospera Corporation's devices?
Among its 2 most recently registered devices, Prospera Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Prospera Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Prospera Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prospera Corporation in the registry?
The most recently registered devices listed for Prospera Corporation include ELECTRONIC PULSE MASSAGER TENS ELECTRONIC PULSE MASSAGER and PROSPERA OTC TENS ELECTRONIC PULSE MASSAGER.