Jenoptik Laser, Optik, Systeme GmbH
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- Devices
- 1
What Jenoptik Laser, Optik, Systeme GmbH makes
Jenoptik Laser, Optik, Systeme GmbH manufactures the JENASCAN, a medical imaging device designed for ophthalmic applications, likely used in retinal or corneal diagnostics.
The JENASCAN is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Jenascan Ref K980001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jenoptik Laser, Optik, Systeme GmbH have in the registry?
The registry currently lists 1 device for Jenoptik Laser, Optik, Systeme GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jenoptik Laser, Optik, Systeme GmbH's devices?
Among its 1 most recently registered device, Jenoptik Laser, Optik, Systeme GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Jenoptik Laser, Optik, Systeme GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jenoptik Laser, Optik, Systeme GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jenoptik Laser, Optik, Systeme GmbH in the registry?
The most recently registered devices listed for Jenoptik Laser, Optik, Systeme GmbH include JENASCAN.