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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 (361)

Page 4 of 8
DeviceModel / ReferenceRegistriesClassStatus
Visalys Veneer 28413-23S
FDA UDI
Class IIUnknown
Panasil 11781
FDA UDI
Class IIActive
Visalys Core 13860
FDA UDI
Class IIActive
Panasil 14706
FDA UDI
Class IIActive
Visalys Veneer 28421L
FDA UDI
Class IIUnknown
Visalys CemCore 13574
FDA UDI
Class IIActive
Panasil 1341111
FDA UDI
Class IIUnknown
Visalys Temp 13783
FDA UDI
Class IIActive
Mixing Tips 17226
FDA UDI
Class IActive
Panasil 13490
FDA UDI
Class IIUnknown
Visalys Veneer 28411M
FDA UDI
Class IIUnknown
Panasil 1356111
FDA UDI
Class IIUnknown
Panasil 13415
FDA UDI
Class IIActive
Panasil 28126
FDA UDI
Class IIActive
Visalys Core 13865
FDA UDI
Class IIActive
Panasil S13400
FDA UDI
Class IIActive
Panasil 1341511
FDA UDI
Class IIUnknown
Panasil 11120
FDA UDI
Class IIActive
Syringe tips 17207
FDA UDI
Class IActive
Panasil 13481
FDA UDI
Class IIUnknown
Panasil 13555
FDA UDI
Class IIUnknown
Visalys Veneer 28411L
FDA UDI
Class IIUnknown
Panasil 28145
FDA UDI
Class IIActive
Mixing Tips 17254
FDA UDI
Class IActive
Profisil 14824
FDA UDI
Class IIActive
Futar 11932
FDA UDI
Class IIActive
Mixing Tips 22011
FDA UDI
Class IUnknown
Visalys Veneer 28454
FDA UDI
Class IIUnknown
Futar 11967
FDA UDI
Class IIActive
Panasil 1355111
FDA UDI
Class IIUnknown
Application Tips 15022
FDA UDI
Class IActive
Panasil 13565
FDA UDI
Class IIUnknown
Futar 28276
FDA UDI
Class IIActive
Mixing Tips 17235
FDA UDI
Class IActive
Profisil 14830
EUDAMEDFDA UDI
Class IIActive
Visalys Veneer 28445S
FDA UDI
Class IIUnknown
Mixing Tips 17240
FDA UDI
Class IActive
Futar 1192811
FDA UDI
Class IIUnknown
Visalys Temp 13849
FDA UDI
Class IIActive
Visalys Veneer 28444M
FDA UDI
Class IIUnknown
Visalys Core 13863
FDA UDI
Class IIUnknown
Visalys Temp 13782
FDA UDI
Class IIActive
Intraoral Tips 17221
FDA UDI
Class IActive
Futar 11912
FDA UDI
Class IIActive
Panasil 1178111
FDA UDI
Class IIUnknown
Visalys Veneer 28423M
FDA UDI
Class IIUnknown
Visalys Flow 15033
FDA UDI
Class IIActive
Mixing Tips 17249
FDA UDI
Class IActive
Futar 11908
FDA UDI
Class IIUnknown
Visalys CemCore Try In Paste 13592
FDA UDI
Class IIActive

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