Aidi MultiMargin Dental Implant

AIDI MultiMargin belongs to the AIDI dental implant range for supporting replacement teeth in the upper or lower jaw. The system uses a threaded, root-form implant and a separate prosthetic…

Registry build 21.09.26

AIDI MultiMargin belongs to the AIDI dental implant range for supporting replacement teeth in the upper or lower jaw. The system uses a threaded, root-form implant and a separate prosthetic abutment.

The implant body is tapered, with an internal hexagonal connection for the restorative assembly. Straight abutments provide cement-retained or screw-retained restoration options.

Listed Item

AIDI Bioperfect® MultiMargin® Implant 4.7mm x 13.5mm, 3.5mm Platform (Practice Building Kit)

Materials and Surface

The AIDI range includes Grade 4 titanium and Ti-6Al-4V ELI titanium-alloy components. The implant surface uses soluble blast media based on tricalcium phosphate and hydroxyapatite. Material and dimensions depend on the selected component; the listed MultiMargin implant is one example within the family.

7manufacturers in China registered for this device type
24catalogue numbers in this listing
2510(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 Aidi MultiMargin Dental Implant
Listed by Aidi Biomedical, LLC, United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
510(k) K101755
Record published 2019-10-30

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Aidi MultiMargin Dental Implant
Catalogue number Size Status
IDI-1247-135-A In distribution
IDI-1247-160 In distribution
IDI-1254-160-A In distribution
IDI-1247-105 In distribution
IDI-1247-088-A In distribution
IDI-1254-088 In distribution
IDI-1254-105-0 In distribution
IDI-1247-105-A In distribution
IDI-1254-088-A In distribution
IDI-1247-105-0 In distribution
IDI-1247-088-0 In distribution
IDI-1254-160-0 In distribution
IDI-1254-105-A In distribution
IDI-1247-135 In distribution
IDI-1247-160-0 In distribution
IDI-1247-160-A In distribution
IDI-1247-088 In distribution
IDI-1254-135 In distribution
IDI-1254-135-0 In distribution
IDI-1254-088-0 In distribution
IDI-1247-135-0 In distribution
IDI-1254-105 In distribution
IDI-1254-160 In distribution
IDI-1254-135-A 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
K123861 2013-12-12
K101755 2010-11-22

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