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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 4 of 70
DeviceModel / ReferenceRegistriesClassStatus
3m™ Espe™ PO-96
FDA UDI
Class IActive
Filtek™ 4863A3
FDA UDI
Class IIActive
RelyX™ 3505L
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ L-56
FDA UDI
Class IActive
Bair Hugger™ 62200
FDA UDI
Class IIActive
3m™ 1840
FDA UDI
Class IIActive
3m™ Espe™ 801202
FDA UDI
Class IActive
Lava™ 4714BL-LT
FDA UDI
Class IIUnknown
3M™ ESPE™ MDI Standard Square Head and Collar 1.8 mm x 13 mm
FDA UDI
Class IIUnknown
3m™ 12157S
FDA UDI
Class IIActive
3M™ Littmann® 8570
FDA UDI
Class IIActive
3M™ Tegaderm™ 1650
FDA UDI
Class IActive
3M™Filtek™ 6120N
FDA UDI
Class IIActive
3M™ Littmann® 2298
FDA UDI
Class IActive
Ioban™ 2 6635
FDA UDI
Class IIActive
3M™ ACE™ Brand 207514
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ U-67
FDA UDI
Class IActive
3M™ ACE™ Brand 909002
FDA UDI
Class IActive
Filtek™ 6033B2
FDA UDI
Class IIUnknown
3M™ Tegaderm™ 1684
FDA UDI
Class IActive
3m™ Espe™ 940335
FDA UDI
Class IActive
Paradigm™ 1481OA3
FDA UDI
Class IIActive
Lava™ 3114BL-LT
FDA UDI
Class IIActive
3M™ Tegaderm™ 90805
FDA UDI
Class IActive
3M™ Littmann® 8838
FDA UDI
Class IIActive
Bair Hugger™ 54500
FDA UDI
Class IIActive
Imprint™ II Garant™ 9579
FDA UDI
Class IIActive
Paradigm™ 5513J
FDA UDI
Class IIActive
3M™ Littmann® Cardiology IV™ 6190
FDA UDI
Class IActive
3M™ Steri-Drape™ Craniotomy Drape with Ioban™ 6687
FDA UDI
Class IIActive
3M™ Tegaderm™ 90003
FDA UDI
Class IActive
3M™ Micropore™ 1533-1
FDA UDI
Class IActive
3M™ Nexcare™ 731
FDA UDI
Class IActive
3M™ Littmann® 2454
FDA UDI
Class IActive
3m™ 8149F
FDA UDI
Class IIActive
3M™ Red Dot™ 2670-5
FDA UDI
Class IIActive
Attest™ 1492V
FDA UDI
Class IIActive
3M™ Tegaderm™ 1624W
FDA UDI
Class IActive
3M™ Tegaderm™ 1837-2100
FDA UDI
Class IActive
3m™ Espe™ DLR7
FDA UDI
Class IActive
3M™ Bair Hugger™ 57501
FDA UDI
Class IIActive
3M™ Steri-Drape™ Craniotomy Pack with Ioban™ 6687P
FDA UDI
Class IIActive
Nexcare™ 778
FDA UDI
Class IActive
3M™ Littmann® Classic III™ 5831
FDA UDI
Class IActive
Filtek™ 4862U-S
FDA UDI
Class IIActive
3M™ Bair Hugger™ 58501
FDA UDI
Class IIActive
Paradigm™ 1481D3
FDA UDI
Class IIActive
Bair Hugger™ 11101
FDA UDI
Class IIActive
3M™ Steri-Strip™ B1557
FDA UDI
Class IActive
Comply™ SteriGage™ 1243A
FDA UDI
Class IIActive

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.