Medical Device Manufacturer · US , St. Petersburg , FL

Lenstec, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2005

Total

Cleared

Denied

Lenstec, Inc. has 6 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.

Historical record: 6 cleared submissions from 2005 to 2016. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Lenstec, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.

Lenstec, Inc. is one of 12968 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lenstec, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 18, 2026