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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 48 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Unitek™	900325	FDA UDI	Class I	Active
Filtek™	6033D2	FDA UDI	Class II	Unknown
3M™ Littmann® Classic III™	5831	FDA UDI	Class I	Active
Lava™	3112A2-HT	FDA UDI	Class II	Unknown
RelyX™	7614B0.5T	FDA UDI	Class II	Active
3M™ Unitek™	900519	FDA UDI	Class I	Active
Filtek™	6020A3	FDA UDI	Class II	Active
3m™ Espe™	940530	FDA UDI	Class I	Active
Vanish™	12149L	FDA UDI	Class II	Active
Lava™	5074B1-LT	FDA UDI	Class II	Active
Littmann®	3100BU	FDA UDI	Class II	Active
Steri-Drape™	9048	FDA UDI	Class II	Active
CavityShield™	12141	FDA UDI	Class II	Unknown
3M™ Micropore™	2270S-1	FDA UDI	Class I	Active
3M™ Unitek™	900431	FDA UDI	Class I	Active
Paradigm™	2710B3-S	FDA UDI	Class II	Unknown
3M™ Micropore™	1532-2	FDA UDI	Class I	Active
3M™ ESPE™ Paradigm™ Nano Hybrid Universal Restorative	1481A2-S	FDA UDI	Class II	Active
Futuro™	71055EN	FDA UDI	Class II	Unknown
3M™ Littmann®	6232	FDA UDI	Class I	Active
Bair Paws™	83101	FDA UDI	Class II	Unknown
3M™ Nexcare™	SFP34	FDA UDI	Class I	Active
Filtek™	6028D3B	FDA UDI	Class II	Active
3M™ Unitek™	900322	FDA UDI	Class I	Active
Ioban™ 2	6648	FDA UDI	Class II	Active
3m™	1157C	FDA UDI	Class II	Active
Steri-Drape™	9036	FDA UDI	Class II	Active
3M™ Durapore™	1538S-2	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1541SB	FDA UDI	Class I	Active
Steri-Drape™	9004	FDA UDI	Class II	Active
Steri-Drape™	9072	FDA UDI	Class II	Active
3M™ Tegaderm™	16006	FDA UDI	Class I	Active
3M™ Nexcare™ Tegaderm™	H1624	FDA UDI	Class I	Active
Comply™	1233LF	FDA UDI	Class II	Active
Lava™	2912B1-LT	FDA UDI	Class II	Active
Curos Jet™	CFJ5-250	FDA UDI	U	Active
3M™ Filtek™	6550A2	FDA UDI	Class II	Active
3M™ Tegaderm™	3584	FDA UDI	Class I	Active
Filtek™	6028A3E	FDA UDI	Class II	Active
3M™ Littmann®	8570	FDA UDI	Class II	Active
3m™ Espe™	940541	FDA UDI	Class I	Active
3m™ Espe™	DUR4	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2167	FDA UDI	Class I	Active
3M™ Micropore™	1532S-1	FDA UDI	Class I	Active
3M™ Unitek™	900326	FDA UDI	Class I	Active
Steri-Drape™	1090	FDA UDI	Class II	Active
Lava™	5072A2-LT	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6238	FDA UDI	Class I	Active
Paradigm™	1481A2	FDA UDI	Class II	Active
3M™ Nexcare™	791-1PK	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.