Acueity, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Viaduct Microendoscope And Accessories Ref K011189
Regimes: 510(k) Registry: 510(k)Viaduct Miniscope And Accessories Ref K040949
Regimes: 510(k) Registry: 510(k)Excisor Bioptome, Model 01-0004 Ref K032847
Regimes: 510(k) Registry: 510(k)Acueity Medical Light Source Ref K032430
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acueity, Inc. have in the registry?
The registry currently lists 4 devices for Acueity, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acueity, Inc.'s devices?
Among its 4 most recently registered devices, Acueity, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Acueity, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Acueity, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acueity, Inc. in the registry?
The most recently registered devices listed for Acueity, Inc. include VIADUCT MICROENDOSCOPE AND ACCESSORIES, VIADUCT MINISCOPE AND ACCESSORIES, EXCISOR BIOPTOME, MODEL 01-0004 and ACUEITY MEDICAL LIGHT SOURCE.