Hans Gevder
Country not established
- Devices
- 1
What Hans Gevder makes
Hans Gevder manufactures an oculopressor, a device used to apply controlled pressure to the eye, typically for diagnostic or therapeutic procedures such as tonometry or intraocular pressure measurement.
The company’s portfolio is regulated under FDA 510(k) clearance in the United States. The device is listed in the FDA’s 510(k) database, adhering to U.S. medical device classification standards. The manufacturer is based in the United States.
Catalogue
Oculopressor Ref K832477
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hans Gevder have in the registry?
The registry currently lists 1 device for Hans Gevder. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hans Gevder's devices?
Among its 1 most recently registered device, Hans Gevder has devices listed in FDA 510(k) (1 device).
What are the newest devices from Hans Gevder in the registry?
The most recently registered devices listed for Hans Gevder include OCULOPRESSOR.