Osang LLC
United Statesfrom the FDA registration address FDA establishment FEI 3020885868
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
OHC COVID-19 Antigen Self Test Ref K241313
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020885868
- Address
- 625 Fair Oaks Ave Ste 360, S Pasadena, CA, 91030
Frequently asked questions
How many devices does OSANG LLC have in the registry?
The registry currently lists 2 devices for OSANG LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list OSANG LLC's devices?
Among its 2 most recently registered devices, OSANG LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do OSANG LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for OSANG LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from OSANG LLC in the registry?
The most recently registered devices listed for OSANG LLC include OHC COVID-19 Antigen Self Test and QuickFinder COVID-19/Flu Antigen Self Test / QuickFinder COVID-19/Flu Antigen Pro Test.