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3M COMPANY

United States·US-MF-000014086

Last updated September 17, 2026

What 3M COMPANY makes

3M COMPANY manufactures a range of medical devices including preformed dental crowns, dental composite resins, mechanical external stethoscopes, patient surgical drapes, hypoallergenic skin adhesive tapes, exudate-absorbent dressings, external circulating-air core temperature regulation system pads, and resin dental inlays. They also produce orthopedic supports such as the FUTURO™ Wraparound Ankle Support, FUTURO™ Night Wrist Support, and FUTURO™ Comfort Elbow Support with Pressure Pads.

The company's portfolio includes Class I, Class II, and U devices, which are listed in the EUDAMED and FDA UDI registries. 3M COMPANY is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does 3M COMPANY manufacture?

3M COMPANY produces a variety of medical devices including preformed dental crowns, dental composite resins, mechanical external stethoscopes, patient surgical drapes, hypoallergenic skin adhesive tapes, exudate-absorbent dressings, temperature regulation pads, and resin dental inlays. They also manufacture orthopedic supports like the FUTURO™ Wraparound Ankle Support and FUTURO™ Night Wrist Support.

Where is 3M COMPANY based?

3M COMPANY is based in the United States. The company operates from its headquarters located in the US, where it designs, manufactures, and distributes its medical devices to various markets.

Which regulatory registries list 3M COMPANY's devices?

3M COMPANY's medical devices are listed in the EUDAMED and FDA UDI registries. These databases track medical devices to ensure proper identification, tracking, and regulation throughout their lifecycle in the respective markets.

How are 3M COMPANY's devices classified?

3M COMPANY's medical devices are classified as Class I, Class II, and U devices. Class I devices pose the lowest risk, Class II devices require more regulatory controls, and U devices are unclassified. This classification determines the level of regulatory oversight each product receives.

AI-generated from registry data and not verified by a human reviewer.

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.

The 3M Company has 2 recall records, with the earliest initiated on 2025-04-10 and the most recent on 2025-04-22. The statuses recorded are open and classified. The reasons given for the recalls are: a notice was issued to clarify flow rates related to the inlet fluid temperature, and a field action to clarify flow rates and inlet fluid temperatures along with the location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

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.