Medi-Ked, Inc.
Country not established
- Devices
- 1
What Medi-Ked, Inc. makes
Medi-Ked, Inc. makes medical devices such as the Kendrick Extrication Device.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kendrick Extrication Device Ref K781761
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Ked, Inc. have in the registry?
The registry currently lists 1 device for Medi-Ked, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Ked, Inc.'s devices?
Among its 1 most recently registered device, Medi-Ked, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medi-Ked, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medi-Ked, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Ked, Inc. in the registry?
The most recently registered devices listed for Medi-Ked, Inc. include KENDRICK EXTRICATION DEVICE.