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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 14 of 70

Device	Model / Reference	Registries	Class	Status
3M™ ESPE™ Protemp™	50600CA	FDA UDI	Class I	Active
3m™ Espe™	940641	FDA UDI	Class I	Active
3m™	EXD-993	FDA UDI	Class II	Active
3M™ Littmann®	8870	FDA UDI	Class II	Active
3M™ Littmann®	2114R	FDA UDI	Class I	Active
Adper™	51102	FDA UDI	Class II	Active
3M™ Unitek™	900311	FDA UDI	Class I	Active
Ranger™	29700	FDA UDI	Class I	Active
Clinpro™	12627SP	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5861	FDA UDI	Class I	Active
3M™ Micropore™	1530-0	FDA UDI	Class I	Active
3M™ Filtek™	6555A2-S	FDA UDI	Class II	Active
3M™ Micropore™	2770K-1	FDA UDI	Class I	Active
3M™ Transpore™	1527-136	FDA UDI	Class I	Active
3M™ Tegaderm™	3593	FDA UDI	Class I	Active
Filtek™	6029AT	FDA UDI	Class II	Active
3M™ ESPE™ Clinpro™ Sealant and Adper™ Prompt™ Trial Kit	12626TP	FDA UDI	Class II	Active
Vitremer™	3303C2	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-76	FDA UDI	Class I	Active
3M™ Unitek™	900512	FDA UDI	Class I	Active
Attest™	41482VF	FDA UDI	Class II	Active
3m™ Espe™	940532	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-55	FDA UDI	Class I	Active
VFlex™	1805	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5868	FDA UDI	Class I	Active
3M™ ESPE™ MDI Standard Square Head and Collar	1.8 mm x 10 mm	FDA UDI	Class II	Unknown
3M™ ESPE™ Iso-Form™	L-71	FDA UDI	Class I	Active
Lava™	5072C2-LT	FDA UDI	Class II	Active
3m™	9667L	FDA UDI	Class I	Active
Bair Hugger™	81103	FDA UDI	Class II	Active
Filtek™	4863A1	FDA UDI	Class II	Active
Vitremer™	3303B2	FDA UDI	Class II	Active
3m™ Espe™	66	FDA UDI	Class I	Active
3M™ ESPE™ MDI Collared Intermediate O-Ball	2.1 mm x 13 mm	FDA UDI	Class II	Unknown
Paradigm™	3710A2	FDA UDI	Class II	Unknown
3M™ Medipore™	2863	FDA UDI	Class I	Active
Steri-Drape™	9058	FDA UDI	Class II	Active
Lava™	5074A1-LT	FDA UDI	Class II	Active
3M™ Unitek™	907014	FDA UDI	Class I	Active
3M™ Unitek™	900234	FDA UDI	Class I	Active
3m™	9661L	FDA UDI	Class I	Active
Filtek™	6021B3	FDA UDI	Class II	Active
3m™ Espe™	5707SD	FDA UDI	Class I	Active
RelyX™	7614A5	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-66	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6240	FDA UDI	Class I	Active
Steri-Drape™	1095	FDA UDI	Class II	Active
3M™ Cavilon™	5050G	FDA UDI	Class I	Active
Bair Paws™	83201	FDA UDI	Class II	Unknown
3M™ Unitek™	907041	FDA UDI	Class I	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.