Medical Device Manufacturer · US , Verona , NJ

Biopsybell S.R.L. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Biopsybell S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Verona, US.

Last cleared in 2023. Active since 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Biopsybell S.R.L. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Maytal Doo and Isemed S.R.L..

Biopsybell S.R.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biopsybell S.R.L.

4 devices

1-4 of 4

Data Source

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

Last updated: May 15, 2026