Electromedical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Electromedical Products, Inc. makes
Electromedical Products, Inc. manufactures transcranial electrical stimulation devices, including the ALPHA-STIM 2000 and its variants (ALPHA-STIM 350, ALPHA-STIM CS). These devices are designed for non-invasive neuromodulation, typically used in clinical settings for conditions such as chronic pain, anxiety, and sleep disorders.
The company’s portfolio is regulated under FDA Class II devices, with each model authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Alpha-Stim 350 Ref K881753
Regimes: 510(k) Registry: 510(k)Alpha-Stim Cs Ref K903014
Regimes: 510(k) Registry: 510(k)Alpha-Stim 2000 Ref K831144
Regimes: 510(k) Registry: 510(k)Alpha-Stim 350 Ref K831145
Regimes: 510(k) Registry: 510(k)Alpha-Stim Cs Ref K896948
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electromedical Products, Inc. have in the registry?
The registry currently lists 5 devices for Electromedical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electromedical Products, Inc.'s devices?
Among its 5 most recently registered devices, Electromedical Products, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Electromedical Products, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Electromedical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electromedical Products, Inc. in the registry?
The most recently registered devices listed for Electromedical Products, Inc. include ALPHA-STIM 350, ALPHA-STIM CS and ALPHA-STIM 2000.