IDS Insight Dental Implant System

3.5x10mm Bone Level Screw-Retained Finished System

Registry build 21.09.26
7manufacturers in China registered for this device type
22catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZE
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Basic (Chengdu) Medical Device Co., Ltd. Chengdu Sichuan Contract manufacturer 1
Dongguan Xinlonghong Hardware Co., Ltd. Dongguan Guangdong Contract manufacturer 1
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
BIO Concept Co., Ltd. Changzhou Jiangsu Manufacturer 5

Record

Regulatory record for IDS Insight Dental Implant System
Listed by Titan Implant Systems, LLC
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Record published 2017-08-09
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Sizes Length 8 to 12 mm; width 3.5 to 5.4 mm

Catalogue Numbers

Catalogue numbers for IDS Insight Dental Implant System
Catalogue number Size Status
380112 Tissue Level In distribution
351010 3.5x10mm Bone Level Screw-Retained Finished System In distribution
460108 Tissue Level In distribution
461010 4.6x10mm Bone Level Screw-Retained Finished System In distribution
380108 Tissue Level In distribution
541008 5.4x8mm Bone Level Screw-Retained Finished System In distribution
540012 Bone Level In distribution
351012 3.5x12mm Bone Level Screw-Retained Finished System In distribution
380110 Tissue Level In distribution
381012 3.8x12mm Bone Level Screw-Retained Finished System In distribution
461012 4.6x12mm Bone Level Screw-Retained Finished System In distribution
541010 5.4x10mm Bone Level Screw-Retained Finished System In distribution
460112 Tissue Level In distribution
540112 Tissue Level In distribution
461008 4.6x8mm Bone Level Screw-Retained Finished System In distribution
381010 3.8x10mm Bone Level Screw-Retained Finished System In distribution
351008 Bone Level Screw-Retained Finished System In distribution
380008 Length 8 mm In distribution
460110 Tissue Level In distribution
350112 Tissue Level In distribution
541012 5.4x12mm Bone Level Screw-Retained Finished System In distribution
381008 3.8x8mm Bone Level Screw-Retained Finished System In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 920
Osstem Implant System Osstem Implant Co., Ltd. 788
Magicore InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 744
Implant, Endosseous, Root-Form Southern Implants (PTY) Ltd 608
ITL Dental Emery Enterprises Inc. 603
Magicore S InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 560
Friadent® Dentsply Implants Manufacturing GmbH 525
Sphero Block Normo Rhein 83 SRL 489
Neobiotech Implant System Neobiotech Co., Ltd. 483
KJ Mini Implant System Kjmeditech.co., Ltd. 448
Ritter Dental Implant System Ritter Implants GmbH & Co. KG 418
Leone SPA Leone SPA 404

Showing 12 of 2,762. All products under Implant, Endosseous, Root-Form

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P800035 2001-10-04 PERI-OSS Curasan AG
P860012 1988-10-28 ALVEOFORM TM BIOGRAFT Collagen Corp.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer