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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 26 of 70

Device	Model / Reference	Registries	Class	Status
3m™ Espe™	6UL6	FDA UDI	Class I	Active
Steri-Drape™	1081PD	FDA UDI	Class II	Active
Steri-Drape™	9079	FDA UDI	Class II	Active
Lava™	2012A1-LT	FDA UDI	Class II	Active
3M™ Unitek™	900533	FDA UDI	Class I	Active
Red Dot™	2270-50	FDA UDI	Class II	Active
3M™ Unitek™	900246	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-60	FDA UDI	Class I	Active
Bair Paws™	83202	FDA UDI	Class II	Active
Ketac™	3305A3	FDA UDI	Class II	Active
3m™	EXD966-1	FDA UDI	Class II	Active
3m™ Espe™	24	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6171	FDA UDI	Class I	Active
Ketac™	3305A1	FDA UDI	Class II	Active
3m™ Espe™	940314	FDA UDI	Class I	Active
3m™	801202	FDA UDI	Class I	Active
3M™ Medipore™	2962S	FDA UDI	Class I	Active
3M™ Ranger™	24200	FDA UDI	Class II	Active
3M™ Nexcare™	W3588	FDA UDI	Class I	Active
Lava™	5044B1-LT	FDA UDI	Class II	Unknown
3M™ Littmann®	6159	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6204	FDA UDI	Class I	Active
Bair Hugger™	61000	FDA UDI	Class II	Active
3M™ Filtek™	6032B2	FDA UDI	Class II	Active
RelyX™	3535	FDA UDI	Class II	Active
3M™ Filtek™	6555D3	FDA UDI	Class II	Active
Bair Hugger™	40068	FDA UDI	Class II	Active
3m™ Espe™	914014	FDA UDI	Class I	Active
Bair Hugger™	90130	FDA UDI	Class II	Active
Lava™	3114EN	FDA UDI	Class II	Unknown
3M™ Tegaderm™	90647	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5646	FDA UDI	Class I	Active
3m™ Espe™	940643	FDA UDI	Class I	Active
3M™ Unitek™	900345	FDA UDI	Class I	Active
3m™ Espe™	914021	FDA UDI	Class I	Active
Adper™ Scotchbond™	7542	FDA UDI	Class II	Active
Vitremer™	3303P	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6204	FDA UDI	Class I	Active
3M™ Transpore™	1527-118	FDA UDI	Class I	Active
Tegaderm™	1658	FDA UDI	U	Active
Lava™	2012A2-LT	FDA UDI	Class II	Active
3M™ Medipore™	2864	FDA UDI	Class I	Active
3M™ Blenderm™	1525-1	FDA UDI	Class I	Active
3M™ Medipore™	2864S	FDA UDI	Class I	Active
Ranger™	29500	FDA UDI	Class II	Active
Filtek™	6028A2E	FDA UDI	Class II	Active
3m	1860S	FDA UDI	Class II	Active
3M™ Durapore™	1538-0D	FDA UDI	Class I	Active
3M™ Transpore™	1534S-2	FDA UDI	Class I	Active
Steri-Drape™	9085	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.