Kline Technologies, Ltd.
Country not established
- Devices
- 1
What Kline Technologies, Ltd. makes
Kline Technologies, Ltd. manufactures The Kline Applicator, a Class I medical device designed for topical application of substances in clinical or procedural settings.
The device is regulated under FDA 510(k) clearance as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
The Kline Applicator Ref K823517
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kline Technologies, Ltd. have in the registry?
The registry currently lists 1 device for Kline Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kline Technologies, Ltd.'s devices?
Among its 1 most recently registered device, Kline Technologies, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Kline Technologies, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kline Technologies, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kline Technologies, Ltd. in the registry?
The most recently registered devices listed for Kline Technologies, Ltd. include THE KLINE APPLICATOR.