Nvision Medical Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Nvision Medical Corporation makes
Nvision Medical Corporation makes the MAKO 7 device.
The MAKO 7 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
MAKO Device Ref K151275
Regimes: 510(k) Registry: 510(k)Mako 7 Ref K160510
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nvision Medical Corporation have in the registry?
The registry currently lists 2 devices for Nvision Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nvision Medical Corporation's devices?
Among its 2 most recently registered devices, Nvision Medical Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Nvision Medical Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nvision Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nvision Medical Corporation in the registry?
The most recently registered devices listed for Nvision Medical Corporation include MAKO Device and MAKO 7.