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NOGA 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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
600763386

Catalogue (484)

Page 3 of 10
DeviceModel / ReferenceRegistriesClassStatus
Plastic Disc for Ball Attachment B
FDA UDI
Class IIActive
Drill ø3.20mm External Irrigation A
FDA UDI
Class IActive
Anatomic Abutment H3mm L6mm Wide A
FDA UDI
Class IIActive
Screw Removal Kit B
FDA UDI
Class IActive
Axis Implant ø4.20 L16mm B
FDA UDI
Class IIActive
Axis Implant ø3.75 L13mm B
FDA UDI
Class IIActive
CC Direct Plastic Cylinder With Hex. W6mm A
FDA UDI
Class IIActive
15° Temporary Abutment H1mm PEEK A
FDA UDI
Class IIActive
Shouldered Abutment Screw B
FDA UDI
Class IIActive
CAD/CAM Ti Base for Multi Unit B
FDA UDI
Class IIActive
Standatd Healing Cap 6mm A
FDA UDI
Class IIActive
RobiCone Implant ø5 L6mm A
FDA UDI
Class IIActive
CC Anatomic Abutment H2mm L4mm A
FDA UDI
Class IIActive
CC Direct Plastic Cylinder Round A
FDA UDI
Class IIActive
Axis Implant ø5 L11.50mm B
FDA UDI
Class IIActive
Axis Implant ø4.20 L6mm B
FDA UDI
Class IIActive
CAD/CAM Low Temporary M.U Ti Cementing Post B
FDA UDI
Class IIActive
CC Multi-Unit 30° H3mm B
FDA UDI
Class IIActive
Axis Implant ø3.75 L8mm B
FDA UDI
Class IIActive
Standatd Healing Cap 4mm A
FDA UDI
Class IIActive
CC Close Tray Transfer H5mm (purple) A
FDA UDI
Class IActive
15° Esthetic Abutment H2mm Burn-Out B
FDA UDI
Class IIActive
CC 25° Narrow Abutment H0mm A
FDA UDI
Class IIActive
Guided Drill for Ø2.4 L16 Implant A
FDA UDI
Class IActive
Equator Attachment Cap Standard Clear A
FDA UDI
Class IIActive
Guided Pilot Drill Ø2.4 L10 A
FDA UDI
Class IActive
Anatomic Restoration Kit H3mm L6mm A
FDA UDI
Class IIActive
Multi-Unit 17° 3mm B
FDA UDI
Class IIActive
Ratchet A
FDA UDI
Class IActive
1.28 Kit Screwdriver A
FDA UDI
Class IActive
Press Fit Transfer B
FDA UDI
Class IActive
CC Prosthetic Kit B
FDA UDI
Class IActive
Guided Drill for Ø3.3 L13 Implant A
FDA UDI
Class IActive
Axis Implant ø4.20 L10mm B
FDA UDI
Class IIActive
Multi-Unit Plastic Cylinder A
FDA UDI
Class IIActive
RobiCone Implant ø4.20 L8mm A
FDA UDI
Class IIActive
Short Drill ø3.20mm External Irrigation A
FDA UDI
Class IActive
Pixel Crestone Surgical Kit B
FDA UDI
Class IActive
25° Esthetic Abutment H2mm Ti B
FDA UDI
Class IIActive
Guided Robicone Ø3.3-Ø4.2 L8-13 Kit B
FDA UDI
Class IActive
Narrow Solid Abutment H0mm A
FDA UDI
Class IIActive
Ball Attachment 2 mm A
FDA UDI
Class IIActive
25° Temporary Abutment H3mm PEEK A
FDA UDI
Class IIActive
Multi-Unit 30° 2mm B
FDA UDI
Class IIActive
Guided Axis Ø3.3-Ø4.2 L8-13 Kit B
FDA UDI
Class IActive
CC Close Tray Transfer H2mm (purple) A
FDA UDI
Class IActive
Axis Implant ø4.20 L11.50mm B
FDA UDI
Class IIActive
CC Esthetic Abutment H1mm Ti A
FDA UDI
Class IIActive
RobiCone Implant ø6 L6mm A
FDA UDI
Class IIActive
Metal Housing for Plastic Ball Cap A
FDA UDI
Class IIActive

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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