Magicore

744 catalogue numbers from 552M6009, listed by InnoBioSurg Co., Ltd.(IBS implant 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
744catalogue 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 Magicore
Listed by InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.)
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
510(k) K152520
Record published 2018-11-26
Record revised 2020-09-11 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date, serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Magicore
Catalogue number Size Status
552M6009 In distribution
502MC6511B In distribution
453M4507 In distribution
551M5509 In distribution
554M7509B In distribution
501MC5010 In distribution
503M6507B In distribution
501MC5513 In distribution
553MC8008B In distribution
503MC5009 In distribution
501M6010 In distribution
501MC5507 In distribution
554M8008B In distribution
502MC6512 In distribution
501MC5513B In distribution
553M6509 In distribution
503MC5013B In distribution
652M6013 In distribution
502M6007B In distribution
603M5009 In distribution
502M5512B In distribution
452M4007 In distribution
603M5507 In distribution
504MC5509 In distribution
504MC6012B In distribution
553M5011 In distribution
502M5513B In distribution
504M5010B In distribution
503M6511B In distribution
651M6009 In distribution
501M6507B In distribution
503MC6011B In distribution
554M5511 In distribution
502MC5513 In distribution
551M5013 In distribution
502MC6513B In distribution
554MC7507B In distribution
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503M5009B In distribution
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601M5013 In distribution
552M5513 In distribution
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551M6511 In distribution
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652M6507 In distribution
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602M5009 In distribution

Showing 250 of 300 catalogue numbers.

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
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
Ankylos® Dentsply Implants Manufacturing GmbH 391

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