Vesticon
Country not established
- Devices
- 1
What Vesticon makes
Vesticon manufactures the EPLEY OMNIAX, a device designed for vestibular rehabilitation and the treatment of benign paroxysmal positional vertigo (BPPV). This device is intended for use in clinical settings to perform repositioning maneuvers under controlled conditions.
The EPLEY OMNIAX is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Epley Omniax Ref K071973
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vesticon have in the registry?
The registry currently lists 1 device for Vesticon. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vesticon's devices?
Among its 1 most recently registered device, Vesticon has devices listed in FDA 510(k) (1 device).
What are the newest devices from Vesticon in the registry?
The most recently registered devices listed for Vesticon include EPLEY OMNIAX.