Odin Medical Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Polestar N-10 Ref K010850
Regimes: 510(k) Registry: 510(k)Rf Tent Ref K022157
Regimes: 510(k) Registry: 510(k)Flexicoil - Malleable Receive-Only Surface Coil Ref K020601
Regimes: 510(k) Registry: 510(k)Polestar N-20 Ref K032541
Regimes: 510(k) Registry: 510(k)Starshield V3 Rf Trnt Ref K050237
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odin Medical Technologies, Ltd. have in the registry?
The registry currently lists 5 devices for Odin Medical Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odin Medical Technologies, Ltd.'s devices?
Among its 5 most recently registered devices, Odin Medical Technologies, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Odin Medical Technologies, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Odin Medical Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odin Medical Technologies, Ltd. in the registry?
The most recently registered devices listed for Odin Medical Technologies, Ltd. include POLESTAR N-10, RF TENT, FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL and POLESTAR N-20.