Phakos is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Phakos - FDA 510(k) Cleared Devices
Recent clearances: MIRA Adapter, Endocular Viewing Lenses and Silicone Ring, Frigitronics adapter
4
Total
4
Cleared
0
Denied
Phakos has 4 FDA 510(k) cleared medical devices. Based in Montreuil, FR.
Historical record: 4 cleared submissions from 2017 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Phakos Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Phakos
4 devices