IQ IMPLANTS LTD

FDA Device Registration & Listing · Omer Southern, IL · Registration 3010610960

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010610960
FEI Number
3010610960
Entity Name
IQ IMPLANTS LTD
City/State/Country
Omer Southern, IL
Establishment Address
Taashur 9, Omer Southern 84965, IL
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
IQ IMPLANTS LTD (Owner Number: 10045610)
Owner / Operator Contact Address
Taashur 9, Omer, IL-D 84965, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Short Drills with External Irrigation Drill Extender External Stoppers Trephine Drill Conical Drills with Internal Irrigation Cylindrical Drills Internal Irrigated Drills with Internal Irrigation Countersink Marking Drill Internal Irrigation Punch Drill Conical Drills with External Irrigation Lance Pilot Drill Drill Extender Internal Drills with External Irrigation Marking Drill External Irrigation Short Drills with Internal Irrigation Ratchet Wrench Hex Driver 1.77mm Hex Drivers 2.5mm for Ratchet Wrench Hex Drivers 1.25 mm for Ratchet Wrench Parallel Guide Short/Long Plastic Castable Abutments Hand Hex Drivers 1.25 Implant Analog Impression Transfer (for open tray ,closed tray) Universal Torque Straight Abutments with Cuff Slim Healing Caps MASTER Implant Healing Cap for Aesthetic Abutment Slim Straight Abutments Connection Abutments SMART Implant Straight Anatomic Abutments Healing Caps Ball Abutments Aesthetic Abutments Straight Abutments Angled Abutments 15 Degrees Easy Lock Abutments UCLA Abutment titanium base Anatomic Angled Abutments 25 Degrees Angled Abutments 25 Degrees Slim Angled Abutment 15 Degrees Anatomic Angled Abutments 15 Degrees

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZA Drill, Dental, Intraoral Dental Class 1 872.4130 2013-12-08
NDP Accessories, Implant, Dental, Endosseous Dental Class 1 872.3980 2013-12-08
DZE Implant, Endosseous, Root-Form Dental Class 2 872.3640 2013-12-08
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2013-12-08

Official Correspondent

No official correspondent registered.

US Agent Details

GREGORY TREPETIN Business: IQ IMPLANTS USA LLC Email: gt@iqimplants.com Phone: (855) 7471010

Related Public Records

Same Entity

IQ IMPLANTS LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K081806 Idi Biomedical, LLC IDI IMPLANT SYSTEM 2008-11-07
K120793 Z-Systems AG Z-LOOK3 EVO SLM 2012-12-21
K130140 Intra-Lock International INTRA-LOCK OP DENTAL IMPLANT 2013-08-01
K925778 Nobelpharma USA, Inc. BRANEMARK SYSTEM LAB. AND EDUCATIONAL ACCESSORIES 1993-04-14
K903999 O Co., Inc. OBUTMENT HB 1992-02-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment SP, Cat. No. 30-70101 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0014-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0015-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0016-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment SU, Cat. No. 30-70104 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.
Z-0017-2022 Paltop Advanced Dental Solutions Ltd 5, Ha-Shita Caesarea Israel 1
Scan Abutment PCA, Cat. No. 30-70105 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient s chewing function.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010610960. Last updated year: 2026. Please use registration number 3010610960 when referencing this establishment in official correspondence.
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