Inolex Corp./Div of Biomedical
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Enteric 20 Ref K771703
Regimes: 510(k) Registry: 510(k)Transette System/Collection & Transp Ref K802563
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inolex Corp./Div of Biomedical have in the registry?
The registry currently lists 2 devices for Inolex Corp./Div of Biomedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inolex Corp./Div of Biomedical's devices?
Among its 2 most recently registered devices, Inolex Corp./Div of Biomedical has devices listed in FDA 510(k) (2 devices).
What risk classes do Inolex Corp./Div of Biomedical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inolex Corp./Div of Biomedical's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Inolex Corp./Div of Biomedical in the registry?
The most recently registered devices listed for Inolex Corp./Div of Biomedical include ENTERIC 20 and TRANSETTE SYSTEM/COLLECTION & TRANSP.