Tyrell, Inc.
Country not established
- Devices
- 1
What Tyrell, Inc. makes
Tyrell, Inc. manufactures the ZENO, a medical device designed for [specific clinical purpose or function not provided—assumed non-disclosure; omit if no detail].
The ZENO is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Zeno Ref K043377
510(k) 510(k)
Frequently asked questions
How many devices does Tyrell, Inc. have in the registry?
The registry currently lists 1 device for Tyrell, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tyrell, Inc.'s devices?
Among its 1 most recently registered device, Tyrell, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tyrell, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tyrell, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tyrell, Inc. in the registry?
The most recently registered devices listed for Tyrell, Inc. include ZENO.