Lentechs, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lentechs, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lentechs, LLC has 1 FDA 510(k) cleared medical devices. Based in Columbus, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Lentechs, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Lentechs, LLC
1 devices