Designer Frames
Country not established
- Devices
- 1
What Designer Frames makes
Designer Frames manufactures spectacle frames, including custom and ready-to-wear designs for prescription and non-prescription eyewear.
The company’s 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 manufacturer is based in the United States.
Catalogue
Spectacle Frame Ref K933874
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Designer Frames have in the registry?
The registry currently lists 1 device for Designer Frames. Devices recorded under merged duplicate company entries are counted once.
Which registries list Designer Frames's devices?
Among its 1 most recently registered device, Designer Frames has devices listed in FDA 510(k) (1 device).
What risk classes do Designer Frames's devices fall under?
Among its 1 most recently registered device, the classes recorded for Designer Frames's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Designer Frames in the registry?
The most recently registered devices listed for Designer Frames include SPECTACLE FRAME.