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Kettenbach GmbH & Co. KG

Germany·DE-MF-000005014

Last updated May 30, 2026

What Kettenbach GmbH & Co. KG makes

Kettenbach GmbH & Co. KG produces dental materials and tools, including silicone and other dental impression materials, dental composite resins, and professional-grade tooth-desensitizing coatings. Their portfolio also includes temporary crowns and bridges, single-use mixing nozzles and application tools, and disposable impression trays. Specific products include flowable composites, try-in pastes, and specialized mixing tips for dental procedures.

The company’s devices are classified as Class I, Class II, or Class IIa under EU and U.S. regulations, with listings in the EUDAMED database, FDA’s 510(k) clearance records, and the FDA’s Unique Device Identifier (UDI) system. The manufacturer is based in Germany.

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 Kettenbach GmbH & Co. KG primarily manufacture?

Kettenbach GmbH & Co. KG specializes in dental materials and tools. Their portfolio includes silicone and other dental impression materials, dental composite resins, professional tooth-desensitizing coatings, temporary crowns and bridges, and single-use items like mixing nozzles, application tools, and impression trays. These products are designed for use in dental procedures, such as impressions, restorations, and cavity treatments.

Where is Kettenbach GmbH & Co. KG based, and how does that affect their regulatory standing?

Kettenbach GmbH & Co. KG is based in Germany, which means their devices are subject to EU medical device regulations. Their products are classified under EU classifications (Class I, Class II, or Class IIa) and are listed in the EUDAMED database, demonstrating compliance with EU regulatory requirements. Additionally, their devices are also tracked in the FDA’s 510(k) clearance records and UDI system in the U.S., reflecting their global market presence.

Which regulatory registries list Kettenbach GmbH & Co. KG’s devices?

Kettenbach GmbH & Co. KG’s devices are listed in multiple regulatory databases to ensure transparency and compliance. Their products appear in the EUDAMED database, which tracks EU-authorized medical devices, as well as the FDA’s 510(k) clearance records and the FDA’s Unique Device Identifier (UDI) system in the United States. These listings help healthcare professionals and regulators verify the authorized status of their devices.

How are Kettenbach GmbH & Co. KG’s devices classified under EU and U.S. regulations?

Kettenbach GmbH & Co. KG’s devices are classified under EU and U.S. medical device regulations based on their risk levels. In the EU, their products fall into Class I (low risk), Class II (moderate risk), or Class IIa (moderate risk with additional controls). In the U.S., the same classifications apply under FDA guidelines, ensuring appropriate oversight and authorization processes are followed for each device type.

Why do some of Kettenbach GmbH & Co. KG’s devices require single-use applications, like mixing nozzles or impression trays?

Kettenbach GmbH & Co. KG offers single-use devices like mixing nozzles and impression trays to enhance hygiene and reduce cross-contamination in dental settings. Single-use items are designed for one-time application, minimizing the risk of bacterial transfer between patients. This approach aligns with strict infection control protocols in dentistry, ensuring safety and compliance with regulatory standards for reusable and disposable medical devices.

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

Information

Country
Germany
Address
7, Im Heerfeld , Eschenburg, Germany
LinkedIn
—
Facebook
—
Phone
+49 2774 705 0
PRRC Contact
Maximilian Meier
EUDAMED SRN
DE-MF-000005014
FDA FEI Number
—
DUNS Number
316803246

Catalogue (360)

Page 1 of 8
DeviceModel / ReferenceRegistriesClassStatus
ProphyProtect 14940
EUDAMED
Class IActive
Visalys Flow 15032
FDA UDI
Class IIActive
Kisol 22301
FDA UDI
Class IUnknown
Silginat 13848
FDA UDI
Class IIUnknown
Mixing Tips 17247
FDA UDI
Class IActive
Mixing Tips 17217
FDA UDI
Class IActive
Futar 11925
FDA UDI
Class IIUnknown
Panasil 1350511
FDA UDI
Class IIUnknown
Visalys Veneer 28415S
FDA UDI
Class IIUnknown
Panasil 28300
FDA UDI
Class IIActive
Visalys Veneer 28413M
FDA UDI
Class IIUnknown
Visalys Veneer 28400
FDA UDI
Class IIUnknown
Visalys Veneer 28432S
FDA UDI
Class IIUnknown
Visalys Veneer 28435M
FDA UDI
Class IIUnknown
Futar 11927
FDA UDI
Class IIUnknown
Mixing Tips 17238
FDA UDI
Class IActive
Visalys CemCore Try In Paste 13593
FDA UDI
Class IIActive
Panasil 1350111
FDA UDI
Class IIUnknown
Profisil 14826
FDA UDI
Class IIActive
Mixing Tips 17244
FDA UDI
Class IActive
Mixing Tips 17236
FDA UDI
Class IActive
Visalys Veneer 28443M
FDA UDI
Class IIUnknown
Panasil 2830011
FDA UDI
Class IIUnknown
Visalys Fill 15005
FDA UDI
Class IIActive
Panasil 13400
FDA UDI
Class IIUnknown
Panasil 13461
FDA UDI
Class IIActive
Futar 28277
FDA UDI
Class IIActive
Visalys Veneer 28414M
FDA UDI
Class IIUnknown
Intraoral Tips 17223
FDA UDI
Class IActive
Futar 1193211
FDA UDI
Class IIUnknown
Panasil 13411
FDA UDI
Class IIActive
Application Tips 15023
FDA UDI
Class IActive
Endo Tips 17224
FDA UDI
Class IActive
Visalys Veneer 28443S
FDA UDI
Class IIUnknown
Visalys Flow 15031
FDA UDI
Class IIActive
Visalys Fill 15004
FDA UDI
Class IIActive
Profisil 14827
FDA UDI
Class IIActive
Visalys Temp 13781US
FDA UDI
Class IIUnknown
Futar 28278
FDA UDI
Class IIActive
Visalys Core 13871
FDA UDI
Class IIActive
Visalys CemCore Try In Paste 13590
FDA UDI
Class IIActive
Multi Tray 17750
FDA UDI
Class IActive
Visalys Core 13866
FDA UDI
Class IIActive
Visalys Veneer 28433-43M
FDA UDI
Class IIUnknown
Visalys Veneer 28451
FDA UDI
Class IIUnknown
Panasil 13551
FDA UDI
Class IIActive
Visalys Veneer 28412L
FDA UDI
Class IIUnknown
Visalys Fill 15003
FDA UDI
Class IIActive
Visalys Veneer 28424L
FDA UDI
Class IIUnknown
Visalys Veneer 28431M
FDA UDI
Class IIUnknown

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