Redwood Biotech, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Redi-Screen Ref K000979
Regimes: 510(k) Registry: 510(k)Redi-Test Pcp Ref K991698
Regimes: 510(k) Registry: 510(k)Redi-Test Thc Ref K990870
Regimes: 510(k) Registry: 510(k)Redi-Screen Ref K993100
Regimes: 510(k) Registry: 510(k)Redi-Test Methamphetamine Ref K991504
Regimes: 510(k) Registry: 510(k)Redi-Test Cocaine Ref K991110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Redwood Biotech, Inc. have in the registry?
The registry currently lists 6 devices for Redwood Biotech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Redwood Biotech, Inc.'s devices?
Among its 6 most recently registered devices, Redwood Biotech, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Redwood Biotech, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Redwood Biotech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Redwood Biotech, Inc. in the registry?
The most recently registered devices listed for Redwood Biotech, Inc. include REDI-SCREEN, REDI-TEST PCP, REDI-TEST THC and REDI-TEST METHAMPHETAMINE.