ARi ExCon Implant

ARi ExCon Implant is a commercially pure Grade 4 titanium dental implant with a sandblasted and acid-etched surface. It is placed in the upper or lower jaw as the supporting substructure…

Registry build 21.09.26

ARi ExCon Implant is a commercially pure Grade 4 titanium dental implant with a sandblasted and acid-etched surface. It is placed in the upper or lower jaw as the supporting substructure for dental restoration.

Normal-thread and deep-thread configurations are available. Separate abutments connect the implant to single or multiple prosthetic restorations.

Healing and Restorative Components

Cover screws protect the fixture connection, while healing abutments shape the emerging gum profile. Temporary abutments support provisional restorations; final restorative options include cement- or screw-retained prostheses and angled abutments. The related abutments and screws use titanium alloy.

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 ARi ExCon Implant
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) K231967
Record published 2024-02-06
Record revised 2026-03-24 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for ARi ExCon Implant
Catalogue number Size Status
ARIE355074 In distribution
ARIE355094 In distribution
ARIE284094 In distribution
ARIE323596 In distribution
ARIE283596 In distribution
ARIE284096 In distribution
ARIE385096 In distribution
ARIE385094 In distribution
ARIE385574 In distribution
ARIE324596 In distribution
ARIE354596 In distribution
ARIE324074 In distribution
ARIE324594 In distribution
ARIE283576 In distribution
ARIE355076 In distribution
ARIE354576 In distribution
ARIE323574 In distribution
ARIE385596 In distribution
ARIE324094 In distribution
ARIE385576 In distribution
ARIE385594 In distribution
ARIE324574 In distribution
ARIE354574 In distribution
ARIE324576 In distribution
ARIE324076 In distribution
ARIE385074 In distribution
ARIE355096 In distribution
ARIE284076 In distribution
ARIE283594 In distribution
ARIE323576 In distribution
ARIE283574 In distribution
ARIE324096 In distribution
ARIE354594 In distribution
ARIE323594 In distribution
ARIE385076 In distribution
ARIE284074 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