Carre Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Carre Technologies, Inc. makes
Carre Technologies, Inc. manufactures the Hexoskin Medical System, a Class II medical device identified by the model number 7100-00016.
The Hexoskin Medical System is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. Carre Technologies is based in the United States.
Catalogue
Hexoskin Medical System (7100-00016) Ref K243981
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carre Technologies, Inc. have in the registry?
The registry currently lists 1 device for Carre Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carre Technologies, Inc.'s devices?
Among its 1 most recently registered device, Carre Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Carre Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Carre Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carre Technologies, Inc. in the registry?
The most recently registered devices listed for Carre Technologies, Inc. include Hexoskin Medical System (7100-00016).