Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

3M Deutschland GmbH

US

Last updated May 24, 2026

What 3M Deutschland GmbH makes

The company produces dental materials and tools, including ceramic fabrication materials for dental appliances, silicone and polyether-based impression materials, and dental composites such as glass ionomer cements and resin fillings. It also manufactures single-use cannulas for material injection, mixing nozzles, and hard denture reliners, alongside temporary dental restorative materials like provisional crowns.

These products are authorised as Class I, Class II, or unclassified devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates with a US-based manufacturing presence.

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

Frequently asked questions

What types of medical devices does 3M Deutschland GmbH primarily manufacture?

3M Deutschland GmbH specializes in dental materials and tools. Their portfolio includes ceramic fabrication materials for dental appliances, impression materials like silicone and polyether-based compounds, dental composites such as glass ionomer cements and resin fillings, and single-use cannulas for material injection. They also produce mixing nozzles, hard denture reliners, and temporary restorative materials like provisional crowns.

Where is 3M Deutschland GmbH based, and does it have a manufacturing presence in the US?

While 3M Deutschland GmbH is based in Germany, the company operates with a manufacturing presence in the US. This allows them to produce and distribute their dental devices globally, including those authorised under FDA regulations.

Which regulatory registries list the devices manufactured by 3M Deutschland GmbH?

The devices produced by 3M Deutschland GmbH are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their authorised products, ensuring transparency and compliance with regulatory requirements.

How are the dental devices from 3M Deutschland GmbH classified under FDA regulations?

The dental devices manufactured by 3M Deutschland GmbH are authorised as Class I, Class II, or unclassified (Class U) devices under FDA regulations. The classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety, with Class I being the lowest risk and Class II requiring additional controls.

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

Information

Country
US
Address
—
Website
mmm.com
LinkedIn
—
Facebook
—
Phone
+1(800)634-2249
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
315731711

Catalogue (1444)

Page 5 of 29
DeviceModel / ReferenceRegistriesClassStatus
Impregum™ Penta™ Soft Quick Step Heavy Body 31769
FDA UDI
Class IIActive
3M™ RelyX™ 56864
FDA UDI
Class IActive
3M™ Durapore™ 1538-118
FDA UDI
Class IActive
Clinpro™ Glycine Prophy Powder 67008
FDA UDI
Class IIActive
3M™ Tegaderm™ 1679
FDA UDI
Class IActive
3M™ RelyX™ 56872
FDA UDI
Class IActive
Imprint™ 4 Penta™ Heavy 71494
FDA UDI
Class IIActive
Imprint™ 4 Preliminary 71548
FDA UDI
Class IIActive
Sinfony™ 49690
FDA UDI
Class IIActive
Adper™ Prompt™ L-Pop™ 41926
FDA UDI
Class IIActive
Sinfony™ 49520
FDA UDI
Class IIActive
Ketac™ Molar Aplicap™ 56430
FDA UDI
Class IIActive
Lava™ Plus 69273
FDA UDI
Class IIActive
Photac™ Fil Quick Aplicap™ 61082
FDA UDI
Class IIActive
3m™ 69943
FDA UDI
Class IIActive
Lava™ Esthetic 69334
FDA UDI
Class IIActive
Permadyne™ 30751
FDA UDI
Class IIActive
Sinfony™ 49330
FDA UDI
Class IIActive
Imprint™ 4 Super Quick Heavy 71535
FDA UDI
Class IActive
3M™ RelyX™ 56949
FDA UDI
Class IActive
Sinfony™ 49170
FDA UDI
Class IIActive
Lava™ Frame Shade 68577
FDA UDI
Class IIActive
3M™ Garant™ 71454
FDA UDI
Class IActive
Lava™ Esthetic 69328
FDA UDI
Class IIActive
Ketac™ Bond Aplicap™ 37350
FDA UDI
Class IIActive
3M™ ESPE™ Impregum™ 31767
FDA UDI
Class IActive
Lava™ Plus 69208
FDA UDI
Class IIActive
Photac™ Fil Quick Aplicap™ 61070
FDA UDI
Class IIActive
Lava™ Frame 68591
FDA UDI
Class IIActive
Ketac™ Fil Plus Aplicap™ 55023
FDA UDI
Class IIActive
3M™ Imprint™ 71492
FDA UDI
Class IActive
RelyX™ Unicem 2 Clicker™ 56875
FDA UDI
Class IIActive
3M™ Ketac™ Universal Aplicap™ 61089
FDA UDI
Class IIActive
RelyX™ Unicem 2 Clicker™ 56876
FDA UDI
Class IIActive
Durelon™ 38224
FDA UDI
Class IIActive
RelyX™ Unicem Maxicap™ 56834
FDA UDI
Class IIActive
Dimension™ Penta™ H 36912
FDA UDI
Class IIActive
3M™ RelyX™ 56875
FDA UDI
Class IIActive
Imprint™ 4 Preliminary Penta™ 71521
FDA UDI
Class IIActive
3m™ 69947
FDA UDI
Class IIActive
3m™ CrownBlockA3.5
FDA UDI
Class IIActive
Imprint™ 4 Preliminary Super Quick 71542
FDA UDI
Class IIActive
RelyX™ Unicem 2 Clicker™ 56874
FDA UDI
Class IIActive
Ketac™ Molar Quick Aplicap™ 56363
FDA UDI
Class IIActive
Imprint™ 4 Super Quick Regular 71520
FDA UDI
Class IActive
3M™ Aplicap™ 73050
FDA UDI
Class IActive
Lava™ Plus 69224
FDA UDI
Class IIActive
Ketac™ Cem radiopaque 37220
FDA UDI
Class IIActive
3M™ Aplicap™ 73050
FDA UDI
Class IActive
Lava™ Esthetic 69375
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • 3M Deutschland GmbH Neuss North Rhine-Westphalia · DE FEI 3008512935