Is this your brand? Sign in to claim ownership.

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 7 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Tegaderm™	90616	FDA UDI	Class I	Active
3M™ Clinpro™	7210FF	FDA UDI	Class II	Active
3M™ Cavilon™	3346	FDA UDI	Class I	Active
Futuro™	71055EN	FDA UDI	Class II	Active
3m™ Espe™	914034	FDA UDI	Class I	Active
3M™ Unitek™	907036	FDA UDI	Class I	Active
3M™ Tegaderm™	1665	FDA UDI	U	Active
3m™	7522S	FDA UDI	Class I	Active
3M™ Unitek™	900232	FDA UDI	Class I	Active
Filtek™	6020I	FDA UDI	Class II	Active
Ranger™	24365	FDA UDI	Class II	Active
3M™ Filtek™	6550-CK	FDA UDI	Class II	Active
Ketac™	3305TK	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2120	FDA UDI	Class I	Active
3m™ Espe™	940510	FDA UDI	Class I	Active
Bair Hugger™	54000	FDA UDI	Class II	Active
3M™ Vflex™	1804S	FDA UDI	Class II	Active
3m™ Espe™	DUL4	FDA UDI	Class I	Active
Filtek™	6029WE	FDA UDI	Class II	Active
Paradigm™	3714A3	FDA UDI	Class II	Active
3M™ Nexcare™	AHD-06	FDA UDI	Class I	Active
3m™ Espe™	40	FDA UDI	Class I	Active
3M™ Unitek™	907013	FDA UDI	Class I	Active
Steri-Drape™	9053P	FDA UDI	Class II	Active
Steri-Drape™	1019	FDA UDI	Class II	Active
3M™ Bair Hugger™	90132	FDA UDI	Class II	Active
3M™ Unitek™	900634	FDA UDI	Class I	Active
3m™ Espe™	DUL6	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1549	FDA UDI	Class I	Active
3M™ Littmann®	6179	FDA UDI	Class I	Active
Attest™	1291	FDA UDI	Class II	Active
Ioban™ 2	6648EZSB	FDA UDI	Class II	Active
3m™	1501NG	FDA UDI	Class I	Active
Filtek™	4864C2	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6168	FDA UDI	Class I	Active
3m™ Espe™	6UL4	FDA UDI	Class I	Active
3M™ Nexcare™	586-20PB	FDA UDI	Class I	Active
Filtek™	4866A3	FDA UDI	Class II	Active
3M™ Durapore™	1538-0	FDA UDI	Class I	Active
Vanish™	12151C	FDA UDI	Class II	Active
3M™ Precise™	DS-25	FDA UDI	Class I	Active
3M™ Cavilon™	3344	FDA UDI	Class I	Active
3m™	8180F	FDA UDI	Class II	Active
3M™ ESPE™ MDI One Piece Implant O-Ball Abutment	2.9 mm x10 mm	FDA UDI	Class II	Unknown
3M™ Ranger™	24250	FDA UDI	Class II	Active
3M™ Filtek™	4872A1	FDA UDI	Class II	Active
3M™ Cavilon™	3343	FDA UDI	Class I	Active
Filtek™	6033W	FDA UDI	Class II	Active
Lava™	1334A3-LT	FDA UDI	Class II	Unknown
3M™ ESPE™ Iso-Form™	U-43	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.