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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 54 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Littmann® Cardiology IV™	6163	FDA UDI	Class I	Active
3M™Filtek™	6110W	FDA UDI	Class II	Active
Bair Hugger™	81102	FDA UDI	Class II	Active
Steri-Drape™	9029	FDA UDI	Class II	Active
3M™ Tegaderm™	90605	FDA UDI	Class I	Active
Red Dot™	2271-50	FDA UDI	Class II	Active
3M™ Red Dot™	2560-5	FDA UDI	Class II	Active
Espe™	2000F	FDA UDI	Class II	Active
3M™ ESPE™ Protemp™	50600	FDA UDI	Class I	Active
3M™ Tegaderm™	90600	FDA UDI	Class I	Active
3m™ Espe™	940332	FDA UDI	Class I	Active
Nova Plus®	V2228	FDA UDI	Class II	Active
Ranger™ Novaplus™	24234	FDA UDI	Class II	Active
Attest™	1261P	FDA UDI	Class II	Active
3M™ Attest™	13911	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1542SB	FDA UDI	Class I	Active
Bair Hugger™	57000	FDA UDI	Class II	Active
3M™ Tegaderm™	3589	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5873	FDA UDI	Class I	Active
Red Dot™	2289T	FDA UDI	Class II	Active
3M™ Tegaderm™	9124	FDA UDI	U	Active
Attest™	1295	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6182	FDA UDI	Class I	Active
3M™ ESPE™ MDI One Piece Implant Tapered Abutment	2.9 mm x15 mm	FDA UDI	Class II	Unknown
Steri-Drape™	9002	FDA UDI	Class II	Active
3M™ Steri-Strip™	B1557	FDA UDI	Class I	Active
3M™ Filtek™	6550A1	FDA UDI	Class II	Active
3m™ Espe™	65	FDA UDI	Class I	Active
RelyX™	7614TRT	FDA UDI	Class II	Active
3m™ Espe™	21	FDA UDI	Class I	Active
3m™ Espe™	22	FDA UDI	Class I	Active
3M™ Nexcare™	H3584	FDA UDI	Class I	Active
Filtek™	6028SU	FDA UDI	Class II	Active
3m™ Espe™	940630	FDA UDI	Class I	Active
Lava™	5044A1-HT	FDA UDI	Class II	Unknown
Espe™	1942FR	FDA UDI	Class II	Unknown
Vitrebond™	7510	FDA UDI	Class II	Active
Filtek™	6033XW	FDA UDI	Class II	Active
3M™ Durapore™	1538-1	FDA UDI	Class I	Active
3M™ Multipore™	3730-1	FDA UDI	Class I	Active
Filtek™	6029C2B	FDA UDI	Class II	Active
3M™ Unitek™	900133	FDA UDI	Class I	Active
3M™ Coban™	1586S	FDA UDI	Class I	Active
3M™ Tegaderm™	1882	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5960	FDA UDI	Class I	Active
CavityShield™	12142	FDA UDI	Class II	Unknown
3m™ Espe™	30	FDA UDI	Class I	Active
3M™ Unitek™	900521	FDA UDI	Class I	Active
3M™ Tegaderm™	1686	FDA UDI	Class I	Active
Filtek™	6029A1D	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.