G. Rodenstock Instrumente GmbH
Country not established
- Devices
- 3
What G. Rodenstock Instrumente GmbH makes
G. Rodenstock Instrumente GmbH manufactures ophthalmic laser devices, including the ORION 3001 laser photocoagulator for retinal treatments, the Rodenstock scanning laser ophthalmoscope for retinal imaging, and the Rodenstock laser slitlamp for combined slitlamp and laser applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Orion 3001, Laser Photocoagulator Ref K864063
Regimes: 510(k) Registry: 510(k)Rodenstock Scanning Laser Ophthalmoscope Ref K871268
Regimes: 510(k) Registry: 510(k)Rodenstock Laser Slitlamp Ref K973220
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does G. Rodenstock Instrumente GmbH have in the registry?
The registry currently lists 3 devices for G. Rodenstock Instrumente GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list G. Rodenstock Instrumente GmbH's devices?
Among its 3 most recently registered devices, G. Rodenstock Instrumente GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do G. Rodenstock Instrumente GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for G. Rodenstock Instrumente GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from G. Rodenstock Instrumente GmbH in the registry?
The most recently registered devices listed for G. Rodenstock Instrumente GmbH include ORION 3001, LASER PHOTOCOAGULATOR, RODENSTOCK SCANNING LASER OPHTHALMOSCOPE and RODENSTOCK LASER SLITLAMP.