Carbon Medical Technologies, Inc.
Carbon Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2026, with 2 FDA device recalls on record.
Top product codes for Carbon Medical Technologies, Inc.
FDA recalls by Carbon Medical Technologies, Inc.
- Z-3161-2024 — BiomarC EX Fiducial Marker System, Catalog Number 040165
- Z-1041-2023 — Mammotome MammoStar Biopsy Site Identified, REF STAR1401
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Carbon Medical Technologies, Inc.
- K253598 — InjecSURE Injection System
- K251748 — MammoSTAR Biopsy Site Identifier
- K211590 — Fiducial Marker
- K172227 — Endoscopic Injection Needle
- K133148 — BIOMARC COAXIAL NEEDLE
- K132064 — BIOMARC FIDUCIAL MARKER
- K132708 — BIOMARC FIDUCIAL MARKER
- K130678 — BIOMARC GOLD FIDUCIAL MARKER
- K110772 — BIOMARC FIDUCIAL MARKER
- K100994 — PRELOADED TISSUE MARKER DEVICE
- K070436 — BIOMARC GOLD TISSUE MARKER
- K063193 — MODIFICATION TO BIOMARC TISSUE MARKER
- K042615 — CARBON MEDICAL TECHNOLOGIES ENDOSCOPIC INJECTION NEEDLE
- K042296 — BIOMARC PRELOADED TISSUE MARKER DEVICE
- K032347 — BIOMARC TISSUE MARKER
- K030451 — CARBON MEDICAL TECHNOLOGIES INJECTION NEEDLE
- K021160 — DERMMATRIX SURGICAL MESH
Data sourced from openFDA. This site is unofficial and independent of the FDA.