Biorem
Country not established
- Devices
- 2
What Biorem makes
Biorem manufactures the BIOREM 2000, 3000, and 4000 series devices.
These devices are classified as class U and are listed in the FDA 510(k) registry, with the manufacturer based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Biorem 3000 & 4000 Ref K833454
Regimes: 510(k) Registry: 510(k)Biorem 2000 Ref K822099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biorem have in the registry?
The registry currently lists 2 devices for Biorem. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biorem's devices?
Among its 2 most recently registered devices, Biorem has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Biorem in the registry?
The most recently registered devices listed for Biorem include BIOREM 3000 & 4000 and BIOREM 2000.