Reborn Fixture

50 catalogue numbers from IC1M3508SC, listed by Cybermed Inc., South Korea, 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
50catalogue numbers in this listing
1510(k) clearance

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 Reborn Fixture
Listed by Cybermed Inc., South Korea
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Manufacturer
510(k) K210039
Record published 2022-10-31

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Reborn Fixture
Catalogue number Size Status
IC1M3508SC In distribution
IC1M3510SC In distribution
IC1M3010C In distribution
IC1R5008C In distribution
IC1M3513OC In distribution
IC1M3508C In distribution
IC1M3510OC In distribution
IC1R4508OC In distribution
IC1R4010OC In distribution
IC1R4507C In distribution
IC1R4513OC In distribution
IC1M3510C In distribution
IC1R4013SC In distribution
IC1R4010C In distribution
IC1R4510C In distribution
IC1M3511SC In distribution
IC1M3011C In distribution
IC1M3511OC In distribution
IC1M3513SC In distribution
IC1R4507OC In distribution
IC1R5508C In distribution
IC1R4010SC In distribution
IC1R4013C In distribution
IC1R4011SC In distribution
IC1R4511OC In distribution
IC1R4510OC In distribution
IC1R4007OC In distribution
IC1R5510C In distribution
IC1R4011C In distribution
IC1R4007SC In distribution
IC1R5013C In distribution
IC1R4511C In distribution
IC1M3511C In distribution
IC1R5011C In distribution
IC1R5010C In distribution
IC1M3513C In distribution
IC1R4013OC In distribution
IC1R5511C In distribution
IC1R4007C In distribution
IC1R4513C In distribution
IC1M3508OC In distribution
IC1M3013C In distribution
IC1M3008C In distribution
IC1R5507C In distribution
IC1R4008OC In distribution
IC1R5007C In distribution
IC1R4008SC In distribution
IC1R4011OC In distribution
IC1R4008C In distribution
IC1R4508C 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K210039 2022-01-07

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