Medical Device Manufacturer · IN , Bari Brahmana

Prevest Denpro Limited - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2021

Total

Cleared

Denied

Prevest Denpro Limited has 7 FDA 510(k) cleared medical devices. Based in Bari Brahmana, IN.

Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Prevest Denpro Limited Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.

Prevest Denpro Limited is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Prevest Denpro Limited

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 09, 2026