Remesta Medical Corp.
Country not established
- Devices
- 1
What Remesta Medical Corp. makes
Remesta Medical Corp. manufactures RHYNOSTAT H-12 and V-22 devices.
These products are classified as Class II medical devices and are listed in the FDA 510(k) regulatory registry. The company is based in the United States.
Catalogue
Rhynostat H-12 & V-22 Ref K852349
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Remesta Medical Corp. have in the registry?
The registry currently lists 1 device for Remesta Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remesta Medical Corp.'s devices?
Among its 1 most recently registered device, Remesta Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Remesta Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Remesta Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Remesta Medical Corp. in the registry?
The most recently registered devices listed for Remesta Medical Corp. include RHYNOSTAT H-12 & V-22.