Efop
FranceFDA applicant, unverified
- Devices
- 1
What Efop makes
Efop manufactures non-custom spectacle lenses designed for prescription use, providing corrective vision solutions for patients. These lenses are intended for general optical correction and are available off-the-shelf without custom adjustments.
The company’s products fall under Class I medical devices in the U.S., regulated through the FDA’s 510(k) pathway. These devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory requirements for low-risk optical corrections.
Catalogue
Lens Spectacle Non-Custom (Prescription) Ref K861162
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Efop have in the registry?
The registry currently lists 1 device for Efop. Devices recorded under merged duplicate company entries are counted once.
Which registries list Efop's devices?
Among its 1 most recently registered device, Efop has devices listed in FDA 510(k) (1 device).
What risk classes do Efop's devices fall under?
Among its 1 most recently registered device, the classes recorded for Efop's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Efop in the registry?
The most recently registered devices listed for Efop include LENS SPECTACLE NON-CUSTOM (PRESCRIPTION).