Klinger Medical
Country not established
- Devices
- 1
What Klinger Medical makes
Klinger Medical makes surgical laser systems, such as the MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Model Mc 2100 Nd:yag Surgical Laser System Ref K901340
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Klinger Medical have in the registry?
The registry currently lists 1 device for Klinger Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Klinger Medical's devices?
Among its 1 most recently registered device, Klinger Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Klinger Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Klinger Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Klinger Medical in the registry?
The most recently registered devices listed for Klinger Medical include MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM.