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Sign in to claim this brandAmsel Medical
US
Last updated May 23, 2026
What Amsel Medical makes
Amsel Medical specializes in metallic ligation clips designed for medical occlusion applications. Their primary product, the Amsel Occluder Device, is intended for use in procedures requiring controlled closure or sealing of anatomical structures.
The company’s devices fall under FDA Class II regulation and are listed under the 510(k) and UDI programs. Their products are authorized for use in the United States, where the manufacturer is based.
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 Amsel Medical manufacture?
Amsel Medical specializes in metallic ligation clips, specifically designed for medical occlusion applications. Their primary product, the Amsel Occluder Device, is intended to provide controlled closure or sealing of anatomical structures during surgical procedures.
Where is Amsel Medical based, and where are their devices authorized for use?
Amsel Medical is based in the United States. Their devices are authorized for use in the U.S., where they are regulated under the jurisdiction of the FDA. The company’s focus is on domestic markets, aligning its products with U.S. regulatory requirements.
How are Amsel Medical’s devices classified by regulatory authorities?
Amsel Medical’s devices fall under FDA Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as metallic ligation clips used for occlusion.
Which regulatory registries or programs list Amsel Medical’s devices?
Amsel Medical’s devices are listed under the FDA’s 510(k) premarket notification program and the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with U.S. regulatory standards for medical devices.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (4)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Amsel Occluder Device | 100-200 | FDA UDI | Class II | Active |
| Amsel Occluder Device | K172479 | FDA 510(k) | Class II | Active |
| Amsel Occluder Device | K140932 | FDA 510(k) | Class II | Active |
| Amsel Endo Occluder | K180650 | FDA 510(k) | Class II | Active |
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