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Sign in to claim this brandStorz am Mark GmbH
US
Last updated May 24, 2026
What Storz am Mark GmbH makes
The company manufactures reusable surgical instruments for dental and soft-tissue procedures, including forceps for tooth extraction, periodontal curettes, periosteal elevators, dental elevators, suturing needle holders, and resin carvers for dental restorations. These tools are designed for precision manipulation of soft tissue and dental structures in clinical settings.
The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with several listed in the FDA’s Unique Device Identification (UDI) system. The company operates with a base in the US, adhering to applicable domestic and international medical device regulations.
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 Storz am Mark GmbH manufacture?
Storz am Mark GmbH specializes in reusable surgical instruments primarily for dental and soft-tissue applications. Their portfolio includes tools like surgical soft-tissue manipulation forceps (similar to tweezers), tooth extraction forceps, periodontal curettes (for cleaning gum pockets), periosteal elevators (to separate tissue from bone), dental elevators (for tooth/root removal), suturing needle holders, and dental restoration carvers for resin. These instruments are designed for precision in clinical procedures.
Where is Storz am Mark GmbH based, and does this affect the devices they manufacture?
Storz am Mark GmbH is based in the US, which means their devices are subject to US regulatory requirements, including those set by the FDA. While the company’s headquarters location doesn’t directly influence the design or function of the devices, it does mean their products must comply with US medical device regulations, such as classification under the FDA’s Class I or Class II categories and, in some cases, inclusion in the FDA’s Unique Device Identification (UDI) system.
Which regulatory registries or databases list Storz am Mark GmbH’s devices?
Storz am Mark GmbH’s devices are listed in the FDA’s Unique Device Identification (UDI) system, which is a central registry for tracking medical devices in the US. This system helps ensure traceability and transparency in the supply chain, particularly for Class I and Class II devices. Listing in the UDI system is a requirement for certain devices under FDA regulations, not an endorsement of the company itself.
How are Storz am Mark GmbH’s devices classified under regulatory frameworks?
Storz am Mark GmbH’s devices are classified under the FDA’s regulatory system as either Class I or Class II. Class I devices generally pose the lowest risk and may require less regulatory oversight, while Class II devices involve moderate risk and typically require special controls to ensure safety and effectiveness. Classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with, as outlined in FDA guidelines.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- stoma.de
- —
- —
- [email protected]
- Phone
- 9999999999
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 318268125
Catalogue (1310)
Page 1 of 27| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Stoma® | 5272.11 | FDA UDI | Class I | Active |
| Stoma® | 4422.08 | FDA UDI | Class I | Active |
| Stoma® | 4080.16 | FDA UDI | Class I | Active |
| Stoma® | 12961.00 | FDA UDI | Class I | Active |
| Stoma® | 14136.17 | FDA UDI | Class I | Active |
| Stoma® | 13291.04 | FDA UDI | Class I | Active |
| Stoma® | 5315.03 | FDA UDI | Class I | Active |
| Stoma® | 4035.00 | FDA UDI | Class I | Active |
| Stoma® | 7555.10 | FDA UDI | Class I | Active |
| Stoma® | 879.01 | FDA UDI | Class I | Active |
| Stoma® | 12702.10 | FDA UDI | Class I | Active |
| Stoma® | 3700.00 | FDA UDI | Class I | Active |
| Stoma® | 3501.11 | FDA UDI | Class I | Active |
| Stoma® | 1276.00 | FDA UDI | Class I | Active |
| Stoma® | 14421.02 | FDA UDI | Class I | Active |
| Stoma® | 5206.02 | FDA UDI | Class I | Active |
| Stoma® | 23050.02 | FDA UDI | Class I | Active |
| Stoma® | 7703.10 | FDA UDI | Class I | Active |
| Stoma® | 3805.14 | FDA UDI | Class I | Active |
| Stoma® | 3586.16 | FDA UDI | Class I | Active |
| Stoma® | 4621.25 | FDA UDI | Class I | Active |
| Stoma® | 1037.00 | FDA UDI | Class I | Active |
| Stoma® | 3546.18 | FDA UDI | Class I | Active |
| Stoma® | 7705.00 | FDA UDI | Class I | Active |
| Stoma® | 7084.00 | FDA UDI | Class I | Active |
| Stoma® | 12838.00 | FDA UDI | Class I | Active |
| Stoma® | 14610.08 | FDA UDI | Class I | Active |
| Stoma® | 14053.17 | FDA UDI | Class I | Active |
| Stoma® | 4053.25 | FDA UDI | Class I | Active |
| Stoma® | 7982.00 | FDA UDI | Class I | Active |
| Stoma® | 2075.00 | FDA UDI | Class I | Active |
| Stoma® | 2053.00 | FDA UDI | Class I | Active |
| Stoma® | 867.00 | FDA UDI | Class I | Active |
| Stoma® | 3570.17 | FDA UDI | Class I | Active |
| Stoma® | 14091.17 | FDA UDI | Class I | Active |
| Stoma® | 4705.13 | FDA UDI | Class I | Active |
| Stoma® | 14749.15 | FDA UDI | Class I | Active |
| Stoma® | 14611.03 | FDA UDI | Class I | Active |
| Stoma® | 12216.00 | FDA UDI | Class I | Active |
| Stoma® | 5201.03 | FDA UDI | Class I | Active |
| Stoma® | 14093.17 | FDA UDI | Class I | Active |
| Stoma® | 5110.00 | FDA UDI | Class I | Active |
| Stoma® | 3387.10 | FDA UDI | Class I | Active |
| Stoma® | 4834.00 | FDA UDI | Class I | Active |
| Stoma® | 707.00 | FDA UDI | Class I | Active |
| Stoma® | 33.11 | FDA UDI | Class I | Active |
| Stoma® | 7513.15 | FDA UDI | Class I | Active |
| Stoma® | 14606.02 | FDA UDI | Class I | Active |
| Stoma® | 3336.15 | FDA UDI | Class I | Active |
| Stoma® | 4071.16 | FDA UDI | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Storz Am Mark Gmbh EMMINGEN-LIPTINGEN Baden-Wurttemberg · DE FEI 3001000014