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Sign in to claim this brandKohler Medizintechnik GmbH & Co. KG
US
Last updated May 23, 2026
What Kohler Medizintechnik GmbH & Co. KG makes
Kohler Medizintechnik GmbH & Co. KG manufactures reusable dental and surgical instruments, including tooth/root elevators, tooth extraction forceps, dental surgical scissors, soft-tissue manipulation forceps, hand-held dental retractors, suturing needle holders, periodontal curettes, and periosteal elevators. These tools are designed for use in dental and oral surgery 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.
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 Kohler Medizintechnik GmbH & Co. KG primarily manufacture?
Kohler Medizintechnik GmbH & Co. KG specializes in reusable dental and surgical instruments. Their product range includes tools like dental elevators for tooth or root extraction, tooth extraction forceps, dental surgical scissors, soft-tissue manipulation forceps, hand-held dental retractors, suturing needle holders, periodontal curettes, and periosteal elevators. These instruments are designed specifically for dental and oral surgery procedures.
Where is Kohler Medizintechnik GmbH & Co. KG based?
The company is headquartered in the United States. This location influences its regulatory compliance and reporting requirements, particularly for devices marketed in the US market.
Which regulatory registries or databases list Kohler Medizintechnik GmbH & Co. KG’s devices?
Kohler Medizintechnik GmbH & Co. KG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their Class I medical devices, ensuring transparency and traceability in the healthcare supply chain.
How are Kohler Medizintechnik GmbH & Co. KG’s devices classified under FDA regulations?
All of Kohler Medizintechnik GmbH & Co. KG’s devices fall under Class I classification according to FDA regulations. This classification applies to low-risk medical devices that pose minimal potential harm to users, such as reusable dental instruments. Class I devices typically require general controls (e.g., good manufacturing practices) but may not need pre-market approval.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (1151)
Page 20 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kohdent | 5739 | FDA UDI | Class I | Active |
| Kohdent | 6427 | FDA UDI | Class I | Active |
| Kohdent | 6373 | FDA UDI | Class I | Active |
| Kohdent | 5631 | FDA UDI | Class I | Active |
| Kohdent | 7771 | FDA UDI | Class I | Active |
| Kohdent | 1144 | FDA UDI | Class I | Active |
| Kohdent | 1122 | FDA UDI | Class I | Active |
| Kohdent | 5036 | FDA UDI | Class I | Active |
| Kohdent | 6378 | FDA UDI | Class I | Active |
| Kohdent | 1120 | FDA UDI | Class I | Active |
| Kohdent | 5842 | FDA UDI | Class I | Active |
| Kohdent | 5195 | FDA UDI | Class I | Active |
| Kohdent | 6775 | FDA UDI | Class I | Active |
| Kohdent | 1444 | FDA UDI | Class I | Active |
| Kohdent | 7465 | FDA UDI | Class I | Active |
| Kohdent | 4010 | FDA UDI | Class I | Active |
| Kohdent | 5843 | FDA UDI | Class I | Active |
| Kohdent | 3196 | FDA UDI | Class I | Active |
| Kohdent | 1052 | FDA UDI | Class I | Active |
| Kohdent | 4112 | FDA UDI | Class I | Active |
| Kohdent | 7694 | FDA UDI | Class I | Active |
| Kohdent | 3060 | FDA UDI | Class I | Active |
| Kohdent | 7572 | FDA UDI | Class I | Active |
| Kohdent | 3249 | FDA UDI | Class I | Active |
| Kohdent | 7306 | FDA UDI | Class I | Active |
| Kohdent | 8091P | FDA UDI | Class I | Active |
| Kohdent | 7751 | FDA UDI | Class I | Active |
| Kohdent | 7909 | FDA UDI | Class I | Active |
| Kohdent | 7942 | FDA UDI | Class I | Active |
| Kohdent | 7420 | FDA UDI | Class I | Active |
| Kohdent | 5241 | FDA UDI | Class I | Active |
| Kohdent | 8090 | FDA UDI | Class I | Active |
| Kohdent | 6536 | FDA UDI | Class I | Active |
| Kohdent | 4001 | FDA UDI | Class I | Active |
| Kohdent | 7198 | FDA UDI | Class I | Active |
| Kohdent | 4415 | FDA UDI | Class I | Active |
| Kohdent | 4015 | FDA UDI | Class I | Active |
| Kohdent | 5976 | FDA UDI | Class I | Active |
| Kohdent | 4088 | FDA UDI | Class I | Active |
| Kohdent | 1184 | FDA UDI | Class I | Active |
| Kohdent | 7570 | FDA UDI | Class I | Active |
| Kohdent | 8360 | FDA UDI | Class I | Active |
| Kohdent | 1010 | FDA UDI | Class I | Active |
| Kohdent | 6839 | FDA UDI | Class I | Active |
| Kohdent | 1306 | FDA UDI | Class I | Active |
| Kohdent | 4583 | FDA UDI | Class I | Active |
| Kohdent | 5242 | FDA UDI | Class I | Active |
| Kohdent | 7581 | FDA UDI | Class I | Active |
| Kohdent | 4249 | FDA UDI | Class I | Active |
| Kohdent | 5313 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Kohler Medizintechnik GmbH STOCKACH Baden-Wurttemberg · DE FEI 3007803626