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Sign in to claim this brandNOGA MEDICAL PRODUCTS LTD
US
Last updated May 23, 2026
What NOGA MEDICAL PRODUCTS LTD makes
NOGA Medical Products Ltd manufactures dental implant components, including titanium and cobalt-chromium abutments, CAD/CAM titanium bases, and customizable restoration kits. Their portfolio also includes plastic and gold abutment cylinders, guided countersinks, and motor keys for dental procedures, alongside esthetic abutments designed for specific anatomical fits.
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. The manufacturer 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 NOGA Medical Products Ltd primarily manufacture?
NOGA Medical Products Ltd specializes in dental implant components. Their portfolio includes titanium and cobalt-chromium abutments, CAD/CAM titanium bases, customizable restoration kits, plastic and gold abutment cylinders, guided countersinks, motor keys, and esthetic abutments tailored for specific anatomical fits. These devices are designed to support dental restoration procedures.
Where is NOGA Medical Products Ltd based?
NOGA Medical Products Ltd operates from the United States. The company’s headquarters and manufacturing operations are located within the country, though specific regional offices or production sites may vary.
Which regulatory registries list NOGA Medical Products Ltd’s devices?
NOGA Medical Products Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the United States, allowing healthcare providers and regulators to verify product details.
How are NOGA Medical Products Ltd’s devices classified under FDA regulations?
NOGA Medical Products Ltd’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 600763386
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Noga Medical Products Ltd. SHLOMI Northern · IL FEI 3021630667