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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 1 of 70

Device	Model / Reference	Registries	Class	Status
FUTURO™ Wraparound Ankle Support	47874DABI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47875SPEI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47875NORD	EUDAMED	Class I	Active
FUTURO™ Night Wrist Support	48462DABI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47875DABI	EUDAMED	Class I	Active
FUTURO™ Night Wrist Support	48462SPEI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47876DABI	EUDAMED	Class I	Active
FUTURO™ Night Wrist Support	48462NORD	EUDAMED	Class I	Active
FUTURO™ Comfort Elbow Support with Pressure Pads	47861DABI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47874SPEI	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47876NORD	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47876SPEI	EUDAMED	Class I	Active
Nexcare Skin Crack Care	N19S	EUDAMED	Class I	Active
FUTURO™ Wraparound Ankle Support	47874NORD	EUDAMED	Class I	Active
3M™ Littmann® Classic III™	5803	FDA UDI	Class I	Active
3M™ Unitek™	907024	FDA UDI	Class I	Active
3M™ Durapore™	1538-3	FDA UDI	Class I	Active
Futuro™	71050EN	FDA UDI	Class II	Active
Z100™	5904B3	FDA UDI	Class II	Active
3M™ Transpore™	1527-0	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5839	FDA UDI	Class I	Active
3M™ Nexcare™	732	FDA UDI	Class I	Active
3M™ Tegaderm™	90603	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5962	FDA UDI	Class I	Active
Littmann®	3100NB	FDA UDI	Class II	Active
3m™ Espe™	6LL6	FDA UDI	Class I	Active
Filtek™	6032XW	FDA UDI	Class II	Active
Tegaderm™	1877-2100	FDA UDI	U	Active
3M™ ESPE™ Z100™ Restorative	5904A2	FDA UDI	Class II	Active
Attest™	490	FDA UDI	Class II	Active
3M™ Transpore™	1527-0	FDA UDI	Class I	Active
Bair Hugger™	90132	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2153	FDA UDI	Class I	Active
3M™ Littmann®	2138	FDA UDI	Class I	Active
3M™ ESPE™ MDI One Piece Implant Tapered Abutment	2.9 mm x13 mm	FDA UDI	Class II	Unknown
3M™ Unitek™	900113	FDA UDI	Class I	Active
3M™ Tegaderm™	9546HP	FDA UDI	Class I	Active
3M™ Tegaderm™	90643	FDA UDI	Class I	Active
3M™ Filtek™	749-212	FDA UDI	Class I	Active
3m™	EXD942CP	FDA UDI	Class II	Active
Vanish™	12160M	FDA UDI	Class II	Active
Lava™	2012A3.5-LT	FDA UDI	Class II	Active
3M™ Medipore™	2866	FDA UDI	Class I	Active
Paradigm™	5513	FDA UDI	Class II	Active
3M™ Filtek™	6032A3-S	FDA UDI	Class II	Active
3M™ Bair Hugger™	62200	FDA UDI	Class II	Active
3m™ Espe™	914004	FDA UDI	Class I	Active
3M™ Medipore™	2861	FDA UDI	Class I	Active
3M™ Littmann®	2157	FDA UDI	Class I	Active
Steri-Drape™	1071	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.