Odin Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Odin Technologies, Ltd. makes
Odin Technologies, Ltd. manufactures the NORMA 10, a medical imaging device designed for intraoperative navigation and guidance, and the POLESTAR N-10, a system used for real-time tracking and localization in surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Norma 10 Ref K991243
Regimes: 510(k) Registry: 510(k)Polestar N-10 Ref K002242
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Odin Technologies, Ltd. have in the registry?
The registry currently lists 2 devices for Odin Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Odin Technologies, Ltd.'s devices?
Among its 2 most recently registered devices, Odin Technologies, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Odin Technologies, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Odin Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Odin Technologies, Ltd. in the registry?
The most recently registered devices listed for Odin Technologies, Ltd. include NORMA 10 and POLESTAR N-10.