Plexus Optix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plexus Optix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ethos Aquell (Hioxifilcon A) One-Day Soft (Hydrophilic) Contact Lenses (59% Water)
1
Total
1
Cleared
0
Denied
Plexus Optix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rancho Cordova, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Plexus Optix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pegavision Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Plexus Optix, Inc.
1 devices