Apimeds, Inc.
Country not established
- Devices
- 1
What Apimeds, Inc. makes
Apimeds, Inc. makes the EXTT-101 device.
The EXTT-101 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
Extt-101 Ref K082436
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apimeds, Inc. have in the registry?
The registry currently lists 1 device for Apimeds, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apimeds, Inc.'s devices?
Among its 1 most recently registered device, Apimeds, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Apimeds, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Apimeds, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apimeds, Inc. in the registry?
The most recently registered devices listed for Apimeds, Inc. include EXTT-101.