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Sign in to claim this brandEndoch Inc
US
Last updated May 27, 2026
What Endoch Inc makes
Endoch Inc manufactures single-use and reusable endoscopic devices, including flexible and rigid biopsy forceps, grasping forceps, scissors, and tissue manipulation tools. Their product line also covers reusable and single-use flexible video colonoscopes and gastroscopes designed for gastrointestinal procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Endoch Inc operates from 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 Endoch Inc manufacture?
Endoch Inc specializes in endoscopic devices used primarily for gastrointestinal procedures. Their product line includes single-use and reusable options such as flexible endoscopic biopsy forceps, rigid endoscopic grasping forceps, scissors, and tissue manipulation forceps. They also produce reusable and single-use flexible video colonoscopes and gastroscopes, which are essential tools for visualizing and accessing internal organs during examinations or interventions.
Where is Endoch Inc based?
Endoch Inc is headquartered in the United States. While the exact location isn’t specified, their primary operations and manufacturing are conducted within the country.
Which regulatory registries list Endoch Inc’s devices?
Endoch Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the United States, ensuring traceability and compliance with regulatory requirements.
How are Endoch Inc’s devices classified under FDA regulations?
Endoch Inc’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards due to moderate risk. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as the gastrointestinal tract.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 241382683
Catalogue (355)
Page 5 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoch | DBF-1818OSC | FDA UDI | Class I | Active |
| Endoch | EAI-0507 | FDA UDI | Class I | Active |
| Endoch | EAI-0498 | FDA UDI | Class II | Active |
| Endoch | EAI-0781 | FDA UDI | Class II | Active |
| Endoch | DBF-2318OS | FDA UDI | Class I | Active |
| Endoch | DHB-2316FS | FDA UDI | Class I | Active |
| Endoch | EAI-0504 | FDA UDI | Class I | Active |
| Endoch | DBF-2318AS | FDA UDI | Class I | Active |
| Endoch | DBF-1816OF | FDA UDI | Class I | Active |
| Endoch | EAI-0572 | FDA UDI | Class I | Active |
| Endoch | DBF-1812OFS | FDA UDI | Class I | Active |
| Endoch | EAI-0731 | FDA UDI | Class I | Active |
| Endoch | DBF-1812AF | FDA UDI | Class I | Active |
| Endoch | DBF-1818OS | FDA UDI | Class I | Active |
| Endoch | EAI-0815 | FDA UDI | Class II | Active |
| Endoch | DBF-1812R | FDA UDI | Class I | Active |
| Endoch | DBF-1812FS | FDA UDI | Class I | Active |
| Endoch | EAI-0496 | FDA UDI | Class II | Active |
| Endoch | DHB-2320RS | FDA UDI | Class I | Active |
| Endoch | DBF-1818R | FDA UDI | Class I | Active |
| Endoch | DBF-1816AS | FDA UDI | Class I | Active |
| Endoch | CS-330L | FDA UDI | Class II | Active |
| Endoch | EAI-0708 | FDA UDI | Class I | Active |
| Endoch | EAI-0634 | FDA UDI | Class I | Active |
| Endoch | DBF-2316AFSC | FDA UDI | Class I | Active |
| Endoch | DBF-1816AFS | FDA UDI | Class I | Active |
| Endoch | CS-430 | FDA UDI | Class II | Active |
| Endoch | EAI-0565 | FDA UDI | Class I | Active |
| Endoch | DBF-2323RS | FDA UDI | Class I | Active |
| Endoch | DBF-1818OFSC | FDA UDI | Class I | Active |
| Endoch | DBF-2316FSC | FDA UDI | Class I | Active |
| Endoch | EAI-0757 | FDA UDI | Class I | Active |
| Endoch | DBF-1812O | FDA UDI | Class I | Active |
| Endoch | DGF-2323RT | FDA UDI | Class II | Active |
| Endoch | DBF-2316AS | FDA UDI | Class I | Active |
| Endoch | EAI-0530 | FDA UDI | Class I | Active |
| Endoch | EAI-0758 | FDA UDI | Class I | Active |
| Endoch | EAI-0674 | FDA UDI | Class I | Active |
| Endoch | DBF-1812RSC | FDA UDI | Class I | Active |
| Endoch | DBF-2323F | FDA UDI | Class I | Active |
| Endoch | EAI-0457 | FDA UDI | Class II | Active |
| Endoch | EAI-0471 | FDA UDI | Class II | Active |
| Endoch | DBF-2318R | FDA UDI | Class I | Active |
| Endoch | DHB-2316RS | FDA UDI | Class I | Active |
| Endoch | DBF-1818OF | FDA UDI | Class I | Active |
| Endoch | DBF-2318AFSC | FDA UDI | Class I | Active |
| Endoch | EAI-0528 | FDA UDI | Class I | Active |
| Endoch | EAI-0730 | FDA UDI | Class II | Active |
| Endoch | GS-500 | FDA UDI | Class II | Active |
| Endoch | DHB-2320AFS | FDA UDI | Class I | Active |
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