Aemed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Aemed, Inc. makes
Aemed, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including over-the-counter units like the StimPad OTC and a prescription-grade model (AEMED STIMPAD ACU-TENS, Model 021999) for pain management.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
StimPad OTC Ref K142686
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aemed, Inc. have in the registry?
The registry currently lists 2 devices for Aemed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aemed, Inc.'s devices?
Among its 2 most recently registered devices, Aemed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Aemed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aemed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aemed, Inc. in the registry?
The most recently registered devices listed for Aemed, Inc. include StimPad OTC and AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999.