Biobot Surgical Pte., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biobot Surgical Pte., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: iSR`obot Mona Lisa 2.0, iSR’obot Mona Lisa 2.0, iSR'obot Mona Lisa 1.0
7
Total
7
Cleared
0
Denied
Biobot Surgical Pte., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Last cleared in 2023. Active since 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Biobot Surgical Pte., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biobot Surgical Pte., Ltd.
7 devices
Cleared
Dec 21, 2023
iSR`obot Mona Lisa 2.0
Radiology
140d
Cleared
Dec 22, 2021
iSR’obot Mona Lisa 2.0
Radiology
64d
Cleared
Jul 08, 2021
iSR'obot Mona Lisa 1.0
Radiology
205d
Cleared
May 16, 2017
iSR'obot Biopsy Kit
Radiology
153d
Cleared
Oct 06, 2016
iSR'obot MRI-US Fusion
Radiology
169d
Cleared
Jun 07, 2013
ISR'OBOT MONA LISA
Radiology
64d
Cleared
Aug 12, 2011
ISROBOT MONA LISA
Radiology
91d