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 5 of 13
DeviceModel / ReferenceRegistriesClassStatus
Hahnenkratt 8X7
FDA UDI
Class IActive
Hahnenkratt 42612C5
FDA UDI
Class IActive
Hahnenkratt 60X13
FDA UDI
Class IActive
Hahnenkratt 711X5
FDA UDI
Class IActive
Hahnenkratt 636X5
FDA UDI
Class IActive
Hahnenkratt 64X101
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7105
FDA UDI
Class IActive
Hahnenkratt 6661
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7102
FDA UDI
Class IActive
Hahnenkratt 543G
FDA UDI
Class IActive
Hahnenkratt 42314C3
FDA UDI
Class IActive
Hahnenkratt 719X12
FDA UDI
Class IActive
Hahnenkratt 621C
FDA UDI
Class IActive
Hahnenkratt 6300X5
FDA UDI
Class IActive
E. Hahnenkratt GmbH B5220
FDA UDI
Class IActive
E. Hahnenkratt GmbH 533X4
FDA UDI
Class IActive
Hahnenkratt 568
FDA UDI
Class IActive
E. Hahnenkratt GmbH B6181
FDA UDI
Class IActive
Hahnenkratt 41X7
FDA UDI
Class IActive
Hahnenkratt 45512C3
FDA UDI
Class IActive
Hahnenkratt 42615C3
FDA UDI
Class IActive
Hahnenkratt H757RX30
FDA UDI
Class IActive
Hahnenkratt 10146
FDA UDI
Class IActive
Hahnenkratt 42611
FDA UDI
Class IActive
E. Hahnenkratt GmbH 41X1
FDA UDI
Class IActive
Hahnenkratt 719X06
FDA UDI
Class IActive
Hahnenkratt 4360D10C5
FDA UDI
Class IActive
Hahnenkratt H757RX20
FDA UDI
Class IActive
Hahnenkratt 600C
FDA UDI
Class IActive
Hahnenkratt 42613C5
FDA UDI
Class IActive
Hahnenkratt H751RX30
FDA UDI
Class IActive
Hahnenkratt 10147
FDA UDI
Class IActive
Hahnenkratt 466
FDA UDI
Class IActive
Hahnenkratt 621F
FDA UDI
Class IActive
Hahnenkratt 44603C5
FDA UDI
Class IActive
Hahnenkratt 10055
FDA UDI
Class IActive
Hahnenkratt 60X11
FDA UDI
Class IActive
Hahnenkratt 569
FDA UDI
Class IActive
Hahnenkratt 4360D16C3
FDA UDI
Class IActive
Hahnenkratt 543D
FDA UDI
Class IActive
E. Hahnenkratt GmbH 7316
FDA UDI
Class IActive
Hahnenkratt H751RX16
FDA UDI
Class IActive
Hahnenkratt 600D
FDA UDI
Class IActive
E. Hahnenkratt GmbH 6645
FDA UDI
Class IActive
Hahnenkratt 6740X3KFO
FDA UDI
Class IActive
E. Hahnenkratt GmbH 6700X2
FDA UDI
Class IActive
E. Hahnenkratt GmbH 625
FDA UDI
Class IActive
Hahnenkratt 561
FDA UDI
Class IActive
Hahnenkratt 595
FDA UDI
Class IActive
Hahnenkratt 43004
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