Reganes, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Reganes Disposable Epidural Anesthesia Tray Ref K880181
Regimes: 510(k) Registry: 510(k)Epidural Anesthesia Needles Ref K854816
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reganes, Inc. have in the registry?
The registry currently lists 2 devices for Reganes, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reganes, Inc.'s devices?
Among its 2 most recently registered devices, Reganes, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Reganes, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Reganes, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reganes, Inc. in the registry?
The most recently registered devices listed for Reganes, Inc. include REGANES DISPOSABLE EPIDURAL ANESTHESIA TRAY and EPIDURAL ANESTHESIA NEEDLES.