KJ Submerged System

60 catalogue numbers from ITX-4514, listed by Kjmeditech.co., Ltd., under Implant, Endosseous, Root-Form. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
60catalogue 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 KJ Submerged System
Listed by Kjmeditech.co., Ltd.
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
510(k) K103810
Record published 2019-08-26

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for KJ Submerged System
Catalogue number Size Status
ITX-4514 In distribution
ITX-4510H In distribution
ITX-6010H In distribution
ITX-3511H In distribution
ITX-3512 In distribution
ITX-5014 In distribution
ITX-4014 In distribution
ITX-3511 In distribution
ITX-6014H In distribution
ITX-4008 In distribution
ITX-4511H In distribution
ITX-4510 In distribution
ITX-6010 In distribution
ITX-6008 In distribution
ITX-3509 In distribution
ITX-4009H In distribution
ITX-6011H In distribution
ITX-5009H In distribution
ITX-6012H In distribution
ITX-5012H In distribution
ITX-4010 In distribution
ITX-5011H In distribution
ITX-6011 In distribution
ITX-4014H In distribution
ITX-4509H In distribution
ITX-3512H In distribution
ITX-3508 In distribution
ITX-4508 In distribution
ITX-4009 In distribution
ITX-5008H In distribution
ITX-4508H In distribution
ITX-5014H In distribution
ITX-4012H In distribution
ITX-6008H In distribution
ITX-4509 In distribution
ITX-4011H In distribution
ITX-5009 In distribution
ITX-4011 In distribution
ITX-5010 In distribution
ITX-6009H In distribution
ITX-4010H In distribution
ITX-4514H In distribution
ITX-5010H In distribution
ITX-3508H In distribution
ITX-3509H In distribution
ITX-5011 In distribution
ITX-3514H In distribution
ITX-6012 In distribution
ITX-3510H In distribution
ITX-4012 In distribution
ITX-4008H In distribution
ITX-3510 In distribution
ITX-6014 In distribution
ITX-4511 In distribution
ITX-6009 In distribution
ITX-3514 In distribution
ITX-4512H In distribution
ITX-4512 In distribution
ITX-5012 In distribution
ITX-5008 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