Milling Abutment

Ø6/ C=1/ P=9/ Non-Hex/ Regular

Registry build 21.09.26
7manufacturers in China registered for this device type
36catalogue numbers in this listing
17510(k) clearances naming this product code

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 Milling Abutment
Listed by Megagen Implant Co., Ltd., South Korea
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Repacker / relabeller, Manufacturer, Exporter
510(k) K203554
Record published 2021-11-18
Record revised 2026-07-15 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Milling Abutment
Catalogue number Size Status
TWCN729 In distribution
RCN619 In distribution
TWCN629 In distribution
RCN649 In distribution
RCH649 In distribution
RCN539 In distribution
RCH639 In distribution
RCH549 In distribution
SCN449 In distribution
TWCH619 In distribution
SCN429 In distribution
RCN549 In distribution
TWCN649 In distribution
SCH449 In distribution
RCH539 In distribution
TWCH629 In distribution
TWCH729 In distribution
TWCH749 In distribution
RCH619 In distribution
RCN519 In distribution
TWCN739 In distribution
TWCN719 In distribution
RCH519 In distribution
RCH529 In distribution
RCN629 In distribution
TWCH649 In distribution
RCN639 In distribution
TWCN749 In distribution
TWCH639 In distribution
RCH629 In distribution
TWCN639 In distribution
SCH429 In distribution
TWCH719 In distribution
TWCH739 In distribution
RCN529 In distribution
TWCN619 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
K251232 2026-06-18
K241972 2024-12-27
K231967 2023-12-07
K230618 2023-10-11
K223339 2023-07-18
K211812 2023-01-06
K203554 2021-08-28
K210161 2021-06-22
K192347 2019-11-14
K182448 2019-10-09
K191127 2019-10-08
K150537 2015-07-21
K140091 2014-12-12
K123988 2013-08-15
K123870 2013-03-27
K122231 2012-10-04
K081302 2008-08-15

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