Healing Abutment

45 catalogue numbers from HA7508GR, listed by Arum Dentistry Co., Ltd., 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
45catalogue numbers in this listing
7510(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 Healing Abutment
Listed by Arum Dentistry Co., Ltd., 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) K222131
Record published 2023-03-30

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

Catalogue Numbers

Catalogue numbers for Healing Abutment
Catalogue number Size Status
HA7508GR In distribution
HA4507GR In distribution
HA4008GR In distribution
HA6505GR In distribution
HA4502GR In distribution
HA4006GR In distribution
HA4009GR In distribution
HA6504GR In distribution
HA6509GR In distribution
HA4503GR In distribution
HA4005GR In distribution
HA5507GR In distribution
HA7509GR In distribution
HA5503GR In distribution
HA6503GR In distribution
HA4003GR In distribution
HA4510GR In distribution
HA5506GR In distribution
HA4002GR In distribution
HA5505GR In distribution
HA4505GR In distribution
HA6506GR In distribution
HA4509GR In distribution
HA4504GR In distribution
HA7503GR In distribution
HA7504GR In distribution
HA5509GR In distribution
HA6507GR In distribution
HA7506GR In distribution
HA4004GR In distribution
HA5508GR In distribution
HA7510GR In distribution
HA7502GR In distribution
HA6510GR In distribution
HA5504GR In distribution
HA6508GR In distribution
HA6502GR In distribution
HA4508GR In distribution
HA4506GR In distribution
HA4010GR In distribution
HA7505GR In distribution
HA5502GR In distribution
HA7507GR In distribution
HA5510GR In distribution
HA4007GR 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
K250280 2025-07-23
K241703 2025-02-24
K242753 2025-01-06
K240091 2024-04-26
K230725 2023-07-01
K222131 2022-09-19
K213506 2022-04-06

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