Carbon Medical Technologies, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Carbon Medical Technologies, Inc. has 16 FDA 510(k) cleared medical devices. Based in St, Paul, US.
Latest FDA clearance: Jul 2025. Active since 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Carbon Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Carbon Medical Technologies, Inc.
16 devices
Cleared
Jul 23, 2025
MammoSTAR Biopsy Site Identifier
General & Plastic Surgery
47d
Cleared
Jun 10, 2021
Fiducial Marker
Radiology
17d
Cleared
Aug 23, 2017
Endoscopic Injection Needle
Gastroenterology & Urology
29d
Cleared
May 13, 2014
BIOMARC COAXIAL NEEDLE
General & Plastic Surgery
208d
Cleared
Feb 28, 2014
BIOMARC FIDUCIAL MARKER
Radiology
240d
Cleared
Dec 20, 2013
BIOMARC FIDUCIAL MARKER
General & Plastic Surgery
113d
Cleared
Apr 12, 2013
BIOMARC GOLD FIDUCIAL MARKER
Radiology
30d
Cleared
Apr 28, 2011
BIOMARC FIDUCIAL MARKER
Radiology
38d
Cleared
Apr 30, 2010
PRELOADED TISSUE MARKER DEVICE
General & Plastic Surgery
21d
Cleared
Mar 16, 2007
BIOMARC GOLD TISSUE MARKER
General & Plastic Surgery
29d
Cleared
Nov 21, 2006
MODIFICATION TO BIOMARC TISSUE MARKER
General & Plastic Surgery
32d
Cleared
Nov 05, 2004
CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE
Gastroenterology & Urology
42d