Anodyne
Also registered as Anodyne Corp.
United Statesfrom the FDA registration address FDA FEI 3011654627
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Anolift - Portable & Anolift - Gantry Ref K902141
Regimes: 510(k) Registry: 510(k)Oasis Lacrimal Intubation Set Ref K160710
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011654627
- Address
- 5050 S 2nd St, Milwaukee, WI, 53207
Frequently asked questions
How many devices does Anodyne have in the registry?
The registry currently lists 2 devices for Anodyne. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anodyne's devices?
Among its 2 most recently registered devices, Anodyne has devices listed in FDA 510(k) (2 devices).
What risk classes do Anodyne's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anodyne's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Anodyne in the registry?
The most recently registered devices listed for Anodyne include ANOLIFT - PORTABLE & ANOLIFT - GANTRY and Oasis Lacrimal Intubation Set.