Tellos Medical AB
SwedenFDA applicant, unverified
- Devices
- 1
What Tellos Medical AB makes
Tellos Medical AB makes medical devices such as the Tellos ISQ Buddy.
The company's portfolio, which includes Class I devices, is listed in the FDA 510k registry, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tellos ISQ Buddy Ref K143445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tellos Medical AB have in the registry?
The registry currently lists 1 device for Tellos Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tellos Medical AB's devices?
Among its 1 most recently registered device, Tellos Medical AB has devices listed in FDA 510(k) (1 device).
What risk classes do Tellos Medical AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tellos Medical AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tellos Medical AB in the registry?
The most recently registered devices listed for Tellos Medical AB include Tellos ISQ Buddy.