Vortex Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vortex Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers, MAXReach Laser Probe
2
Total
2
Cleared
0
Denied
Vortex Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chesterfield, US.
Last cleared in 2022. Active since 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vortex Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vortex Surgical, Inc.
2 devices