Flexlens, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Flexlens(Methafilcon A) Ref K962000
Regimes: 510(k) Registry: 510(k)Flexlens 55 Soft (Hydrophilic) Contact Lens Ref K950294
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexlens, Inc. have in the registry?
The registry currently lists 3 devices for Flexlens, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexlens, Inc.'s devices?
Among its 3 most recently registered devices, Flexlens, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Flexlens, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Flexlens, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexlens, Inc. in the registry?
The most recently registered devices listed for Flexlens, Inc. include FLEXLENS(METHAFILCON A), FLEXLENS 55 SOFT (HYDROPHILIC) CONTACT LENS and CONTROLLED PROCESS RELEASE OF FLEXLENS (HEFILCON A).