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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
—
Phone
+1(800)634-2249
PRRC Contact
Harry Janiski
EUDAMED SRN
US-MF-000014086
FDA FEI Number
2110898
DUNS Number
830016148

Catalogue (3490)

Page 13 of 70
DeviceModel / ReferenceRegistriesClassStatus
Vanish™ Varnish 12159M
FDA UDI
Class IIActive
Steri-Drape™ 9027
FDA UDI
Class IIActive
3M™ Bair Hugger™ 37000
FDA UDI
Class IIActive
Red Dot™ 9641
FDA UDI
Class IIActive
3M™ Transpore™ 1527-618
FDA UDI
Class IActive
Red Dot™ 2236
FDA UDI
Class IIActive
"3M™ ESPE™ MDI Max with O-Ball Head and Collar 2.4 mm x 10 mm
FDA UDI
Class IIUnknown
3M™ Durapore™ 1538S-1
FDA UDI
Class IActive
3M™ Nexcare™ SST-1
FDA UDI
Class IActive
3M™ Filtek™ 6555B2
FDA UDI
Class IIActive
RelyX™ 3525
FDA UDI
Class IIActive
Filtek™ 6021A2
FDA UDI
Class IIActive
Futuro™ 71059EN
FDA UDI
Class IIActive
3M™ Littmann® Classic II™ 2155
FDA UDI
Class IActive
Steri-Drape™ 1014
FDA UDI
Class IIActive
3m™ 6550D3
FDA UDI
Class IIActive
3m™ Espe™ ELR3
FDA UDI
Class IActive
Ranger™ 24365
FDA UDI
Class IIActive
Filtek™ 6020A2
FDA UDI
Class IIActive
3M™ Littmann® Cardiology IV™ 6166
FDA UDI
Class IActive
3M™ Littmann® Master Classic II™ 2147
FDA UDI
Class IActive
3m™ Espe™ 940342
FDA UDI
Class IActive
3M™ Littmann® Cardiology IV™ 6186C
FDA UDI
Class IActive
Filtek™ 6028A4D
FDA UDI
Class IIActive
3M™ Unitek™ 907004
FDA UDI
Class IActive
Nova Plus® V2228-3
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ U-61
FDA UDI
Class IActive
Imprint™ 10771J
FDA UDI
Class IIActive
3M™ Nexcare™ 791-2PK
FDA UDI
Class IActive
3m™ Espe™ 2923
FDA UDI
Class IUnknown
3M™ Tegaderm™ 1685NS
FDA UDI
Class IActive
3M™ Filtek™ 6550A2-CP
FDA UDI
Class IIActive
3m™ 1860
FDA UDI
Class IIActive
3M™ Tegaderm™ 90005
FDA UDI
Class IActive
3M™ Steri-Strip™ W8512
FDA UDI
Class IActive
3M™ Steri-Strip™ W8516
FDA UDI
Class IActive
3M™ Littmann® Classic III™ 5835
FDA UDI
Class IActive
3M™ Durapore™ 1538-1
FDA UDI
Class IActive
3M™ Littmann® Cardiology IV™ 6152
FDA UDI
Class IActive
Imprint™ II Garant™ 9578
FDA UDI
Class IIActive
3M™ Medipore™ 3573
FDA UDI
Class IActive
Filtek™ 6020A4
FDA UDI
Class IIActive
Steri-Drape™ 2037
FDA UDI
Class IIActive
Tegaderm™ 1879-2100
FDA UDI
UActive
Steri-Drape™ 9057
FDA UDI
Class IIActive
3M™ Cavilon™ 3346
FDA UDI
Class IActive
3M™ ESPE™ MDI Collared Intermediate O-Ball 2.1 mm x 15 mm
FDA UDI
Class IIUnknown
3M™ ACE™ Brand 900132
FDA UDI
Class IActive
Fast Release Varnish 12158C
FDA UDI
Class IIActive
3M™ Nexcare™ Active™ 511-08
FDA UDI
Class IActive

Related Companies

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Importers

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Notified Bodies

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Authorities

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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.

DateRecall No.ClassStatusReason
Apr 22, 2025Z-2231-2025—open, classified

Notice was issued to clarify flow rates related to the inlet fluid temperature.

Apr 10, 2025Z-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.