Biopsybell S.R.L. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
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.
FDA 510(k) cleared devices by Biopsybell S.R.L.
4 devices
Cleared
Oct 30, 2023
Renova Spine Balloon Catheter
Orthopedic
174d
Cleared
Jan 11, 2021
Marrow-Pack (white)- 11gauge/10cm or 13gauge/10cm, Marrow-Tray (red)-...
General & Plastic Surgery
54d
Cleared
Mar 26, 2018
DISKOM
Orthopedic
49d
Cleared
Feb 07, 2014
MANUAL-BONE-MARROW-BIOPSY-NEEDLES, SEMI-AUTOMATIC-BIOPSY-NEEDLES,...
Gastroenterology & Urology
337d