Biospace Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3003193933
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Inbody AP1 Body Composition Analyzer Ref K023478
Regimes: 510(k) Registry: 510(k)Inbody, Model 3.0 Ref K042528
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Biospace Ref K131064
Regimes: 510(k) Registry: 510(k)Inbody Ref K110689
Regimes: 510(k) Registry: 510(k)Inbody, Models: 270, R20, R20B Ref K092786
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Inbody Ref K130777
Regimes: 510(k) Registry: 510(k)Biospace Body Composition Analyzer Ref K141483
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003193933
- Address
- 13850 CERRITOS CORPORATE DR STE C, Cerritos, CA, 90703
Frequently asked questions
How many devices does BIOSPACE INC. have in the registry?
The registry currently lists 10 devices for BIOSPACE INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BIOSPACE INC.'s devices?
Among its 10 most recently registered devices, BIOSPACE INC. has devices listed in FDA 510(k) (10 devices).
What risk classes do BIOSPACE INC.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for BIOSPACE INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BIOSPACE INC. in the registry?
The most recently registered devices listed for BIOSPACE INC. include INBODY AP1 BODY COMPOSITION ANALYZER, INBODY, MODEL 3.0, BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 and BIOSPACE.