Lindley Company, Inc.
Country not established
- Devices
- 1
What Lindley Company, Inc. makes
Lindley Company, Inc. manufactures the Kangle condom, a barrier contraceptive device designed for male use.
The Kangle condom is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Kangle Condom Ref K871020
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lindley Company, Inc. have in the registry?
The registry currently lists 1 device for Lindley Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lindley Company, Inc.'s devices?
Among its 1 most recently registered device, Lindley Company, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lindley Company, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lindley Company, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lindley Company, Inc. in the registry?
The most recently registered devices listed for Lindley Company, Inc. include KANGLE CONDOM.