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E. Hahnenkratt GmbH

US

Last updated May 23, 2026

What E. Hahnenkratt GmbH makes

E. Hahnenkratt GmbH manufactures reusable dental instruments, including dental mirrors, surgical probes, and matrix bands for dental restorations. Their portfolio also includes preformed root canal posts, laryngeal mirrors, matrix band tensioners, and specialized dental drill bits for pin/post applications. These tools are designed for use in endodontic and restorative dental procedures.

The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States, adhering to applicable domestic regulatory requirements for reusable dental instruments.

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 E. Hahnenkratt GmbH manufacture?

E. Hahnenkratt GmbH specializes in reusable dental instruments. Their product range includes dental mirrors for oral examinations, root canal posts for endodontic treatments, dental surgical probes for precision procedures, and reusable dental matrix bands used in restorative work. They also produce laryngeal mirrors for medical examinations, matrix band tensioners to assist in dental restorations, and specialized pin/post dental drill bits for preparing tooth structures. These devices are designed for use in endodontics and restorative dentistry.

Where is E. Hahnenkratt GmbH based, and what regulatory framework applies to their devices?

E. Hahnenkratt GmbH is based in the United States. Their devices fall under the jurisdiction of the U.S. Food and Drug Administration (FDA). Specifically, these reusable dental instruments are classified as Class I medical devices, which typically pose the lowest risk among FDA-regulated products. This classification means they are subject to general controls, including registration and listing requirements, but may not require pre-market approval or other stringent reviews.

Are E. Hahnenkratt GmbH’s devices listed in any regulatory registries?

Yes, E. Hahnenkratt GmbH’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution and use. Listing in this registry ensures transparency and traceability, which is particularly important for reusable instruments like those produced by the company, as they may be sterilized and reused across multiple procedures.

How are E. Hahnenkratt GmbH’s devices classified under FDA regulations?

E. Hahnenkratt GmbH’s devices are classified as Class I medical devices under FDA regulations. This classification is based on their intended use and risk profile—reusable dental instruments like mirrors, probes, and matrix bands are generally considered low-risk due to their routine, non-invasive applications in dental procedures. Class I devices are subject to FDA’s general controls, which include registration, listing, and adherence to good manufacturing practices, but they do not require pre-market approval or post-market surveillance beyond standard compliance.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
316001098

Catalogue (636)

Page 1 of 13
DeviceModel / ReferenceRegistriesClassStatus
Hahnenkratt 6061
FDA UDI
Class IActive
Hahnenkratt 43604
FDA UDI
Class IActive
Hahnenkratt 10145
FDA UDI
Class IActive
Hahnenkratt 565
FDA UDI
Class IActive
Hahnenkratt 542
FDA UDI
Class IActive
Hahnenkratt 41X150
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7100
FDA UDI
Class IActive
Hahnenkratt 4360D16
FDA UDI
Class IActive
Hahnenkratt 6300X7
FDA UDI
Class IActive
Hahnenkratt 43002
FDA UDI
Class IActive
E. Hahnenkratt GmbH B6240
FDA UDI
Class IActive
Hahnenkratt 719X08
FDA UDI
Class IActive
Hahnenkratt 10134
FDA UDI
Class IActive
Hahnenkratt 8X6
FDA UDI
Class IActive
Hahnenkratt 626A
FDA UDI
Class IActive
Hahnenkratt 543A
FDA UDI
Class IActive
E. Hahnenkratt GmbH 6530X3
FDA UDI
Class IActive
Hahnenkratt 6560
FDA UDI
Class IActive
Hahnenkratt 44702C3
FDA UDI
Class IActive
Hahnenkratt 41X6
FDA UDI
Class IActive
Hahnenkratt B600A
FDA UDI
Class IActive
Hahnenkratt 10336
FDA UDI
Class IActive
Hahnenkratt H750RX26
FDA UDI
Class IActive
Hahnenkratt 41X15
FDA UDI
Class IActive
Hahnenkratt 415
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7115
FDA UDI
Class IActive
Hahnenkratt 626G
FDA UDI
Class IActive
Hahnenkratt 43602C3
FDA UDI
Class IActive
Hahnenkratt 544A
FDA UDI
Class IActive
Hahnenkratt 6080
FDA UDI
Class IActive
Hahnenkratt B442
FDA UDI
Class IActive
Hahnenkratt 542A
FDA UDI
Class IActive
Hahnenkratt 45514C3
FDA UDI
Class IActive
E. Hahnenkratt GmbH 40X102
FDA UDI
Class IActive
Hahnenkratt 625F
FDA UDI
Class IActive
Hahnenkratt 622A
FDA UDI
Class IActive
Hahnenkratt 5200
FDA UDI
Class IActive
Hahnenkratt 43603C5
FDA UDI
Class IActive
Hahnenkratt H951RX06
FDA UDI
Class IActive
Hahnenkratt 467
FDA UDI
Class IActive
Hahnenkratt H757RX22
FDA UDI
Class IActive
Hahnenkratt 4370D10
FDA UDI
Class IActive
Hahnenkratt 633X4
FDA UDI
Class IActive
Hahnenkratt 6861
FDA UDI
Class IActive
Hahnenkratt H956RX14
FDA UDI
Class IActive
E. Hahnenkratt GmbH B6070
FDA UDI
Class IActive
Hahnenkratt 624D
FDA UDI
Class IActive
Hahnenkratt 542F
FDA UDI
Class IActive
Hahnenkratt 421
FDA UDI
Class IActive
Hahnenkratt 6540X3
FDA UDI
Class IActive

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FDA Establishments (1)

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

  • E. Hahnenkratt Gmbh KOENIGSBACH-STEIN Baden-Wurttemberg · DE FEI 4395