Anamar
Country not established
- Devices
- 1
What Anamar makes
Anamar manufactures glass frames and their component parts for eyewear, designed to fit standard optical and non-optical lenses.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Glass Frames & Component Parts Ref K831388
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anamar have in the registry?
The registry currently lists 1 device for Anamar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anamar's devices?
Among its 1 most recently registered device, Anamar has devices listed in FDA 510(k) (1 device).
What risk classes do Anamar's devices fall under?
Among its 1 most recently registered device, the classes recorded for Anamar's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Anamar in the registry?
The most recently registered devices listed for Anamar include GLASS FRAMES & COMPONENT PARTS.