Stephen A. Dunn, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Daily Wear Soft (Hydrophilic) Contact Lens Ref K953807
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stephen A. Dunn, Inc. have in the registry?
The registry currently lists 2 devices for Stephen A. Dunn, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stephen A. Dunn, Inc.'s devices?
Among its 2 most recently registered devices, Stephen A. Dunn, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Stephen A. Dunn, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stephen A. Dunn, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stephen A. Dunn, Inc. in the registry?
The most recently registered devices listed for Stephen A. Dunn, Inc. include DAILY WEAR SOFT (HYDROPHILIC) CONTACT LENS and POLYVUE, SILVER CHORD AND UNISOFT (METHAFILCON A) SPHERICAL, ASPHERICAL, TORIC AND MULTIFOCAL HYDROPHILIC CONTACT LENSE).