Vista Ophthalmics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vista Ophthalmics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vista Ophthalmics Vitrectomy Probe
1
Total
1
Cleared
0
Denied
Vista Ophthalmics, LLC has 1 FDA 510(k) cleared medical devices. Based in Katy, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vista Ophthalmics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Pathways Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vista Ophthalmics, LLC
1 devices