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3M COMPANY

United States·US-MF-000014086

Last updated September 17, 2026

Information

Country: United States
Address: 2510, Conway Avenue, St.Paul, United States
Website: solventum.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)634-2249
PRRC Contact: Harry Janiski
EUDAMED SRN: US-MF-000014086
FDA FEI Number: 2110898
DUNS Number: 830016148

Catalogue (3490)

Page 17 of 70

Device	Model / Reference	Registries	Class	Status
3m™	3402	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6164	FDA UDI	Class I	Active
3M™ ESPE™ MDI One Piece Implant O-Ball Abutment	2.9 mm x13 mm	FDA UDI	Class II	Unknown
Adper™ Scotchbond™	7546	FDA UDI	Class II	Unknown
3m™ Espe™	54	FDA UDI	Class I	Active
3M™ Unitek™	900147	FDA UDI	Class I	Active
Vanish™	12149C	FDA UDI	Class II	Active
3m™	EXD-982	FDA UDI	Class I	Active
3m™ Espe™	E-UR-5	FDA UDI	Class I	Active
Filtek™	6032B2	FDA UDI	Class II	Active
3M™ Tegaderm™	9545HP	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5910C	FDA UDI	Class I	Active
Steri-Drape™	9003	FDA UDI	Class II	Active
SpotOn™	37000	FDA UDI	Class II	Active
Steri-Drape™ Ioban™ 2	6697P001	FDA UDI	Class II	Active
3M™ ESPE™ Filtek™ Supreme Ultra Universal Restorative	6029M	FDA UDI	Class II	Active
3M™ Red Dot™	2268-5	FDA UDI	Class II	Active
3M™ Nexcare™	870-B4	FDA UDI	Class I	Active
3m™	EXD-949	FDA UDI	Class II	Active
Vitremer™	3303MP-A3	FDA UDI	Class II	Active
3m™	2244	FDA UDI	Class II	Active
Imprint™ II Garant™	9379	FDA UDI	Class II	Active
3M™ Unitek™	900511	FDA UDI	Class I	Active
3M™ Medipore™	2862	FDA UDI	Class I	Active
3m™ Espe™	17	FDA UDI	Class I	Active
3M™ Cavilon™	3344ENS	FDA UDI	Class I	Active
3M™ Multipore™	3730-2	FDA UDI	Class I	Active
Filtek™	6033C2	FDA UDI	Class II	Unknown
Curos™	CSA5-250	FDA UDI	U	Active
Comply™	00130LF	FDA UDI	Class II	Active
Steri-Drape™	1077	FDA UDI	Class II	Active
3M™ Ioban™	6648EZ	FDA UDI	Class II	Active
3M™ Micropore™	1530-336	FDA UDI	Class I	Active
Paradigm™	3710E	FDA UDI	Class II	Unknown
Ketac™	3305A2	FDA UDI	Class II	Active
3M™ Unitek™	900531	FDA UDI	Class I	Active
3m™ Espe™	6LR4	FDA UDI	Class I	Active
Filtek™	6020UD	FDA UDI	Class II	Active
3m™ Espe™	64	FDA UDI	Class I	Active
3M™ Microfoam™	1528-4	FDA UDI	Class I	Active
Steri-Drape™	9003	FDA UDI	Class II	Active
3M™Filtek™	6120W	FDA UDI	Class II	Active
Bair Hugger™	89500	FDA UDI	Class II	Active
3M™ Littmann®	2161	FDA UDI	Class I	Active
3M™ Littmann®	2114	FDA UDI	Class I	Active
3M™ Nexcare™	AC-108	FDA UDI	Class I	Active
Filtek™	6028XWB	FDA UDI	Class II	Active
Comply™	1355-18MM	FDA UDI	Class II	Active
Bair Hugger™	53700	FDA UDI	Class II	Active
3m™	42568	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

3M Deutschland GmbH (Medical) DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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
Apr 22, 2025	Z-2231-2025	—	open, classified	Notice was issued to clarify flow rates related to the inlet fluid temperature.
Apr 10, 2025	Z-2483-2025	—	open, classified	Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.