Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
316001098

Catalogue (636)

Page 4 of 13
DeviceModel / ReferenceRegistriesClassStatus
Hahnenkratt 41X16
FDA UDI
Class IActive
Hahnenkratt 726X5
FDA UDI
Class IActive
E. Hahnenkratt GmbH 40X5
FDA UDI
Class IActive
.Hahnenkratt 6730X1
FDA UDI
Class IActive
Hahnenkratt 545C
FDA UDI
Class IActive
E. Hahnenkratt GmbH 5181
FDA UDI
Class IActive
Hahnenkratt 44X113
FDA UDI
Class IActive
Hahnenkratt 720X8
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7302
FDA UDI
Class IActive
Hahnenkratt 545G
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7110
FDA UDI
Class IActive
Hahnenkratt 6071
FDA UDI
Class IActive
Hahnenkratt 442
FDA UDI
Class IActive
Hahnenkratt 10155
FDA UDI
Class IActive
Hahnenkratt 42612
FDA UDI
Class IActive
Hahnenkratt 6550X2
FDA UDI
Class IActive
Hahnenkratt 44604C3
FDA UDI
Class IActive
Hahnenkratt 730X7
FDA UDI
Class IActive
Hahnenkratt 719X14
FDA UDI
Class IActive
Hahnenkratt 43702C3
FDA UDI
Class IActive
Hahnenkratt H757RX18
FDA UDI
Class IActive
Hahnenkratt 623D
FDA UDI
Class IActive
Hahnenkratt 623C
FDA UDI
Class IActive
Hahnenkratt 42312C5
FDA UDI
Class IActive
Hahnenkratt 44601C3
FDA UDI
Class IActive
Hahnenkratt 12
FDA UDI
Class IActive
Hahnenkratt 10035
FDA UDI
Class IActive
Hahnenkratt 6165
FDA UDI
Class IActive
E. Hahnenkratt GmbH 41X4
FDA UDI
Class IActive
Hahnenkratt 626F
FDA UDI
Class IActive
Hahnnkratt 6540X3KFO
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7117
FDA UDI
Class IActive
E. Hahnenkratt GmbH 716X3
FDA UDI
Class IActive
E. Hahnenkratt GmbH 40X151
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7307
FDA UDI
Class IActive
Hahnenkratt 667AF
FDA UDI
Class IActive
Hahnenkratt 625G
FDA UDI
Class IActive
Hahnenkratt 6300X1
FDA UDI
Class IActive
Hahnenkratt 45511
FDA UDI
Class IActive
Hahnenkratt 600F
FDA UDI
Class IActive
Hahnenkratt 43604C3
FDA UDI
Class IActive
E. Hahnenkratt GmbH 719X16
FDA UDI
Class IActive
Hahnenkratt 626D
FDA UDI
Class IActive
E. Hahnenkratt GmbH 41X2
FDA UDI
Class IActive
E. Hahnenkratt GmbH 5183
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7314
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7112
FDA UDI
Class IActive
Hahnenkratt 420
FDA UDI
Class IActive
Hahnenkratt 775X5
FDA UDI
Class IActive
Hahnenkratt 44601C5
FDA UDI
Class IActive

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.

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