Ancie Laboratories
Country not established
- Devices
- 1
What Ancie Laboratories makes
Ancie Laboratories manufactures spectacle prescription lenses designed to correct vision for individual patient needs, including single-vision and multifocal options.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Spectacle Prescription Lenses Ref K853110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ancie Laboratories have in the registry?
The registry currently lists 1 device for Ancie Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ancie Laboratories's devices?
Among its 1 most recently registered device, Ancie Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Ancie Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ancie Laboratories's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ancie Laboratories in the registry?
The most recently registered devices listed for Ancie Laboratories include SPECTACLE PRESCRIPTION LENSES.