M & K Co.
Country not established
- Devices
- 1
What M & K Co. makes
M & K Co. manufactures plastic guides, which are medical devices used to assist in the positioning or alignment of anatomical structures during procedures.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Plastic-Guides Ref K901842
510(k) 510(k)
Frequently asked questions
How many devices does M & K Co. have in the registry?
The registry currently lists 1 device for M & K Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M & K Co.'s devices?
Among its 1 most recently registered device, M & K Co. has devices listed in FDA 510(k) (1 device).
What risk classes do M & K Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for M & K Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from M & K Co. in the registry?
The most recently registered devices listed for M & K Co. include PLASTIC-GUIDES.