T.E.S., Ltd.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What T.E.S., Ltd. makes
T.E.S., Ltd. manufactures the ADVENTURER, a Class I medical device designed for use in specific diagnostic or monitoring applications.
The ADVENTURER is regulated under the FDA’s 510(k) pathway and is listed in the U.S. as a Class I device. The company is based in the United States.
Catalogue
Adventurer Ref K971142
510(k) 510(k)
Frequently asked questions
How many devices does T.E.S., Ltd. have in the registry?
The registry currently lists 1 device for T.E.S., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T.E.S., Ltd.'s devices?
Among its 1 most recently registered device, T.E.S., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do T.E.S., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for T.E.S., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from T.E.S., Ltd. in the registry?
The most recently registered devices listed for T.E.S., Ltd. include ADVENTURER.