Vibrant Health
CanadaFDA applicant, unverified
- Devices
- 3
What Vibrant Health makes
Vibrant Health manufactures medical devices for acupuncture and electroacupuncture, including the AKUPORT M1 and M-2 disposable acupuncture needles, as well as the EAV COMBI-2 device for electroacupuncture therapy. These products are designed for clinical use in pain management and traditional acupuncture treatments.
The company’s portfolio consists of Class II devices, which are regulated under the FDA’s 510(k) clearance process in the United States. These devices are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations.
Catalogue
Akuport M1 Ref K020567
Regimes: 510(k) Registry: 510(k)Akuport M-2 Ref K020568
Regimes: 510(k) Registry: 510(k)Eav Combi-2 Ref K020565
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vibrant Health have in the registry?
The registry currently lists 3 devices for Vibrant Health. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vibrant Health's devices?
Among its 3 most recently registered devices, Vibrant Health has devices listed in FDA 510(k) (3 devices).
What risk classes do Vibrant Health's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vibrant Health's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vibrant Health in the registry?
The most recently registered devices listed for Vibrant Health include AKUPORT M1, AKUPORT M-2 and EAV COMBI-2.