Telesis Corp.
Country not established
- Devices
- 1
What Telesis Corp. makes
Telesis Corp. makes a Fertility Awareness Method Kit.
The Fertility Awareness Method Kit 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
Fertility Awareness Method Kit Ref K801791
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telesis Corp. have in the registry?
The registry currently lists 1 device for Telesis Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telesis Corp.'s devices?
Among its 1 most recently registered device, Telesis Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Telesis Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Telesis Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telesis Corp. in the registry?
The most recently registered devices listed for Telesis Corp. include FERTILITY AWARENESS METHOD KIT.