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Carbon Medical Technologies, Inc.

United States·US-MF-000044355

Last updated September 17, 2026

About

Today, Carbon Medical Technologies (CMT) is one of only five organizations worldwide with a dedicated pyrolytic carbon coating facility, allowing us to engineer and manufacture devices that are durable, dependable, and trusted by clinicians. Over the past three decades, we’ve built a portfolio of clinically proven products that support patients, simplify procedures, and raise the standard of care across multiple specialties.

From the manufacturer's own website. Source

Information

Country: United States
Address: 1290, HAMMOND ROAD, SAINT PAUL, United States
Website: WWW.CARBONMED.COM
LinkedIn: linkedin.com/company/carbon-med-technologies-inc/mycompany
Facebook: facebook.com/Carbon-Medical-Technologies-Inc-109530911330572
Email: [email protected]
Phone: 1 651 653 8512
PRRC Contact: ERIC FURLICH
EUDAMED SRN: US-MF-000044355
FDA FEI Number: 3002619738
DUNS Number: —

Catalogue (111)

Page 1 of 3

Device	Model / Reference	Registries	Class	Status
BiomarC PRO Fiducial Marker	040148	EUDAMED	Class IIb	Active
BiomarC EX Fiducial Marker	040157	EUDAMED	Class IIb	Active
BiomarC PRO Fiducial Marker	040149	EUDAMED	Class IIb	Active
BiomarC EX Fiducial Marker	040146	EUDAMED	Class IIb	Active
BiomarC EX Fiducial Marker	040160	EUDAMED	Class IIb	Active
BiomarC EX Fiducial Marker	040145	EUDAMED	Class IIb	Active
BiomarC Enh Fiducial Marker	040117	EUDAMED	Class IIb	Active
BiomarC Enh Fiducial Marker	040159	EUDAMED	Class IIb	Active
BiomarC Secure Fiducial Marker	040150	EUDAMED	Class IIb	Active
BiomarC Enh Fiducial Marker	040158	EUDAMED	Class IIb	Active
BiomarC®	040122	FDA UDI	Class II	Active
BiomarC®	040240	FDA UDI	Class II	Active
BiomarC®	040229	FDA UDI	Class II	Active
MammoStar™	STAR0833	FDA UDI	Class II	Active
Carbon Bright®	040152	FDA UDI	Class II	Active
BiomarC®	040138	FDA UDI	Class II	Active
MammoStar™	STAR0831	FDA UDI	Class II	Active
MammoStar™	STAR1032	FDA UDI	Class II	Active
Durasphere ®	890-205	FDA UDI	Class II	Active
MammoStar™	STAR1102	FDA UDI	Class II	Active
Carbon Bright®	040151	FDA UDI	Class II	Active
BiomarC®	040230	FDA UDI	Class II	Active
MammoStar™	STAR1402	FDA UDI	Class II	Active
Durasphere ®	890-204	FDA UDI	Class II	Active
ImarC™	040301	FDA UDI	Class II	Unknown
BiomarC ®	040142	FDA UDI	Class II	Active
BiomarC®	040123	FDA UDI	Class II	Active
MammoStar™	STAR1101	FDA UDI	Class II	Active
Durasphere ® EXP	890-216	FDA UDI	Class III	Active
Biomarc® Restore	040156	EUDAMEDFDA UDI	Class II	Active
BiomarC®	040119	FDA UDI	Class II	Unknown
Biomarc ® Restore	040161	FDA UDI	Class II	Active
BiomarC®	040137	FDA UDI	Class II	Active
BiomarC®	040120	FDA UDI	Class II	Active
BiomarC ®	040133	FDA UDI	Class II	Active
BiomarC®	040123	FDA UDI	Class II	Unknown
ImarC™	040210	FDA UDI	Class II	Unknown
BiomarC®	040109	FDA UDI	Class II	Active
BiomarC®	040122	FDA UDI	Class II	Unknown
BiomarC®	040132	FDA UDI	Class II	Unknown
Carbon Bright ®	040166	FDA UDI	Class II	Active
BiomarC®	040315	FDA UDI	Class II	Active
Durasphere ® EXP	890-215	FDA UDI	Class III	Active
BiomarC®	040311	FDA UDI	Class II	Active
BiomarC®	040119	FDA UDI	Class II	Active
MammoStar™	STAR0832	FDA UDI	Class II	Active
MammoStar™	STAR0802	FDA UDI	Class II	Active
MammoStar™	STAR1121	FDA UDI	Class II	Active
ImarC™	040303	FDA UDI	Class II	Unknown
Biomarc ® Restore	040162	FDA UDI	Class II	Active

Related Companies

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jul 26, 2024	Z-3161-2024	—	open, classified	This recall has been initiated due to a failure to provide an MRI Insert that is to be provided to the patient.
Dec 16, 2022	Z-1041-2023	—	terminated	The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell shaped marker pre-loaded in a 14 gauge needle, while the packaging contains STAR1402, a 1x5mm Tribell shaped marker pre-loaded in a 14 gauge needle.