Geuder GmbH
Country not established
Part of Geuder AG
- Devices
- 1
What Geuder GmbH makes
Geuder GmbH manufactures the Geuder Injector, a device designed for the implantation of the Morcher Capsular Tension Ring, used in ophthalmic surgery to support the lens capsule and maintain intraocular stability.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Geuder Injector listed via a 510(k) premarket notification. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geuder GmbH have in the registry?
The registry currently lists 1 device for Geuder GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geuder GmbH's devices?
Among its 1 most recently registered device, Geuder GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Geuder GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Geuder GmbH's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Geuder GmbH in the registry?
The most recently registered devices listed for Geuder GmbH include GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING.