Maquet S.A.
Country not established
- Devices
- 1
What Maquet S.A. makes
Maquet S.A. manufactures the POWERLED Surgical Light System, a Class II medical device designed for illumination during surgical procedures.
The POWERLED Surgical Light System is regulated under the FDA’s 510(k) pathway and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Powerled Surgical Light System Ref K070442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maquet S.A. have in the registry?
The registry currently lists 1 device for Maquet S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maquet S.A.'s devices?
Among its 1 most recently registered device, Maquet S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Maquet S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maquet S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maquet S.A. in the registry?
The most recently registered devices listed for Maquet S.A. include POWERLED SURGICAL LIGHT SYSTEM.