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

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.

510(k) submissions have been managed by Maytal Doo as regulatory consultant.