Gernot Lindner, Lunor-Vertrieb
GermanyFDA applicant, unverified
- Devices
- 1
What Gernot Lindner, Lunor-Vertrieb makes
The company specializes in spectacle frames, which are designed for corrective eyewear and optical devices.
These products fall under Class I medical devices and are listed via the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Spectacle Frames Ref K934301
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gernot Lindner, Lunor-Vertrieb have in the registry?
The registry currently lists 1 device for Gernot Lindner, Lunor-Vertrieb. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gernot Lindner, Lunor-Vertrieb's devices?
Among its 1 most recently registered device, Gernot Lindner, Lunor-Vertrieb has devices listed in FDA 510(k) (1 device).
What risk classes do Gernot Lindner, Lunor-Vertrieb's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gernot Lindner, Lunor-Vertrieb's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gernot Lindner, Lunor-Vertrieb in the registry?
The most recently registered devices listed for Gernot Lindner, Lunor-Vertrieb include SPECTACLE FRAMES.