Siegel Optik
GermanyFDA applicant, unverified
- Devices
- 1
What Siegel Optik makes
Siegel Optik manufactures prescription eyeglass lenses and frames, including standard and specialty optical corrections for vision correction.
Their products are regulated as Class I medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company operates from the United States.
Catalogue
Glasses Ref K931451
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siegel Optik have in the registry?
The registry currently lists 1 device for Siegel Optik. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siegel Optik's devices?
Among its 1 most recently registered device, Siegel Optik has devices listed in FDA 510(k) (1 device).
What risk classes do Siegel Optik's devices fall under?
Among its 1 most recently registered device, the classes recorded for Siegel Optik's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Siegel Optik in the registry?
The most recently registered devices listed for Siegel Optik include GLASSES.