Yehuda Tamari
Country not established
- Devices
- 1
What Yehuda Tamari makes
Yehuda Tamari makes the TAMARI-KAPLITT device.
The TAMARI-KAPLITT is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tamari-Kaplitt Ref K760695
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Yehuda Tamari have in the registry?
The registry currently lists 1 device for Yehuda Tamari. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yehuda Tamari's devices?
Among its 1 most recently registered device, Yehuda Tamari has devices listed in FDA 510(k) (1 device).
What risk classes do Yehuda Tamari's devices fall under?
Among its 1 most recently registered device, the classes recorded for Yehuda Tamari's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Yehuda Tamari in the registry?
The most recently registered devices listed for Yehuda Tamari include TAMARI-KAPLITT.