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

Catalogue (484)

Page 2 of 10
DeviceModel / ReferenceRegistriesClassStatus
Planning Kit B
FDA UDI
Class IActive
Wide Healing Cap 2mm B
FDA UDI
Class IIActive
Axis Implant ø6 L11.50mm B
FDA UDI
Class IIActive
Multi-Unit H1mm A
FDA UDI
Class IIActive
Open Tray Transfer Standard H5mm B
FDA UDI
Class IActive
Healing Cap 6mm A
FDA UDI
Class IIActive
Torque Ratchet B
FDA UDI
Class IActive
CC Direct Plastic Cylinder With Hex. W10mm A
FDA UDI
Class IIActive
Drill ø4.50mm External Irrigation A
FDA UDI
Class IActive
Step Drills with Integral Stopper Dia.2.4 L6mm A
FDA UDI
Class IActive
Massif Implant ø4.20 L11.50mm B
FDA UDI
Class IIActive
CC 15° Angulated Abutment A
FDA UDI
Class IIActive
Drill ø2.50mm External Irrigation A
FDA UDI
Class IActive
Axis Implant ø5 L6mm B
FDA UDI
Class IIActive
Guide 1-3 Sites Case A
FDA UDI
Class IActive
Anatomic Restoration Kit H1mm L8mm A
FDA UDI
Class IIActive
Guided Drill for Ø4.2 L16 Implant A
FDA UDI
Class IActive
Anatomic Healing Cap 2mm A
FDA UDI
Class IIActive
CC Anatomic Abutment H1mm L6mm A
FDA UDI
Class IIActive
MU Analog for printed model B
FDA UDI
Class IIActive
Anatomic Abutment H1mm L8mm B
FDA UDI
Class IIActive
Anatomic Healing Cap 5mm Wide A
FDA UDI
Class IIActive
Step drill ø2.80/2.3mm A
FDA UDI
Class IActive
Step Drills with Integral Stopper Dia.2.4 L8mm A
FDA UDI
Class IActive
Crestone One Piece Implant ø3 L11.50mm B
FDA UDI
Class IIActive
Guided Drill for Ø4.2 L13 Implant A
FDA UDI
Class IActive
RobiCone Implant ø4.20 L13mm A
FDA UDI
Class IIActive
CC CAD/CAM Temporary Ti Cementing Post A
FDA UDI
Class IIActive
CC 15° Esthetic Abutment H1mm Ti A
FDA UDI
Class IIActive
Healing Cap 2mm A
FDA UDI
Class IIActive
Massif Implant ø4.20 L6mm B
FDA UDI
Class IIActive
Guided Bone Mill Ø3.75 A
FDA UDI
Class IActive
Motor key 1.28 Long A
FDA UDI
Class IActive
Hand Tool 2.42 Short A
FDA UDI
Class IActive
Massif Implant ø5 L11.50mm B
FDA UDI
Class IIActive
Axis Implant ø5 L8mm B
FDA UDI
Class IIActive
Screw Removal Burr Guide A
FDA UDI
Class IActive
Spade Marking Drill A
FDA UDI
Class IActive
Anatomic Abutment H3mm L6mm A
FDA UDI
Class IIActive
CC Multi-Unit 17° H3mm B
FDA UDI
Class IIActive
1-72 UNF Tap A
FDA UDI
Class IActive
Multi-Unit 30° 4mm A
FDA UDI
Class IIActive
Equator Attachment Cap Strong Violet A
FDA UDI
Class IIActive
Short Drill ø4.50mm External Irrigation A
FDA UDI
Class IActive
Crestone One Piece Implant ø3.50 L13mm B
FDA UDI
Class IIActive
Equator Abutment H5mm A
FDA UDI
Class IActive
Guided Pilot Drill Ø2.4 L11.5 A
FDA UDI
Class IActive
Short Drill ø2.50mm External Irrigation A
FDA UDI
Class IActive
Axis Implant ø5 L13mm B
FDA UDI
Class IIActive
CC Anatomic Abutment H2mm L6mm Wide A
FDA UDI
Class IIActive

Related Companies

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Authorities

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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