Nk-Optik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Nk-Optik GmbH makes
Nk-Optik GmbH manufactures the Light Coagulator LC 250, a medical device used for laser-based tissue coagulation in ophthalmic procedures, particularly for retinal treatments.
The device falls under FDA Class II regulation and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Light Coagulator Lc 250 Ref K881334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nk-Optik GmbH have in the registry?
The registry currently lists 1 device for Nk-Optik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nk-Optik GmbH's devices?
Among its 1 most recently registered device, Nk-Optik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Nk-Optik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nk-Optik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nk-Optik GmbH in the registry?
The most recently registered devices listed for Nk-Optik GmbH include LIGHT COAGULATOR LC 250.