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