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Sign in to claim this brandFINE SURGICAL INSTRUMENTS INC.
US
Last updated May 30, 2026
What FINE SURGICAL INSTRUMENTS INC. makes
Fine Surgical Instruments Inc. manufactures circumcision clamps, including both reusable and single-use variants. Their primary product is the Gomco Type Circumcision Clamp, designed for medical circumcision procedures.
The company’s devices are classified under Class I and Class II regulations, with all products 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 Fine Surgical Instruments Inc. manufacture?
Fine Surgical Instruments Inc. specializes in circumcision clamps, offering both reusable and single-use versions. Their primary product is the Gomco Type Circumcision Clamp, which is specifically designed for medical circumcision procedures. These devices are intended for use in clinical settings where precision and safety are critical.
Where is Fine Surgical Instruments Inc. based?
Fine Surgical Instruments Inc. is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards, which govern the manufacturing, distribution, and use of its medical devices.
Which regulatory registries list Fine Surgical Instruments Inc.’s devices?
Fine Surgical Instruments Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify device details, such as manufacturer information and classification.
How are Fine Surgical Instruments Inc.’s devices classified under medical regulations?
Fine Surgical Instruments Inc.’s circumcision clamps fall under Class I and Class II regulatory classifications. Class I devices are generally considered low-risk, while Class II devices may pose a moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory oversight required for each product.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- finesurgical.com
- —
- —
- [email protected]
- Phone
- +1(516)292-7400
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 103669727
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Gomco Type Circumcision Clamp | 28-856 | FDA UDI | Class II | Active |
| Gomco Type Circumcision Clamp | 28-855 | FDA UDI | Class II | Active |
| Gomco Type Circumcision Clamp | 903-016 | FDA UDI | Class I | Active |
| Gomco Type Circumcision Clamp | 28-857 | FDA UDI | Class II | Active |
| Gomco Type Circumcision Clamp | 903-014 | FDA UDI | Class I | Active |
| Gomco Type Circumcision Clamp | 28-854 | FDA UDI | Class II | Active |
| Gomco Type Circumcision Clamp | 903-020 | FDA UDI | Class I | Active |
| Gomco Type Circumcision Clamp | 903-018 | FDA UDI | Class I | Active |
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