MDL

Transitional MDL Implant 2.0MM Implant Single 8MM

Registry build 21.09.26
7manufacturers in China registered for this device type
69catalogue numbers in this listing
8510(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 MDL
Listed by Intra-Lock International, United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
510(k) K070601
Record published 2019-06-11
Record revised 2019-06-18 (version 5)

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, manufacturing date
Sizes Angle 15 °
Distribution end date 2025-05-30

Catalogue Numbers

Catalogue numbers for MDL
Catalogue number Size Status
MDL2518S In distribution
MDL2010S In distribution
MDL2013 In distribution
MDL2011 In distribution
MDLOP2515 In distribution
MDL2511 In distribution
MDL2518L In distribution
MDL2518S In distribution
MDL2513 In distribution
MDL2511S In distribution
MDL2510L In distribution
MDL2510S In distribution
MDL2013P In distribution
MDL2513L In distribution
MLD2008S In distribution
MDL2518L In distribution
MDL2011S In distribution
MDL2510 In distribution
MDL2015 In distribution
MDL2515S In distribution
MDL2518 In distribution
MDLOP2513 In distribution
MDL2511L In distribution
MDL2515 In distribution
MDL2015S In distribution
MDL2018 In distribution
MDL2013S In distribution
MDLOP2518 In distribution
MDL2010 In distribution
MDL2515A Angle 15 ° In distribution
MDL2513 In distribution
MDL2513S In distribution
MDL2515L In distribution
MDL2008 In distribution
MDL2515 In distribution
MDL2011 In distribution
MDL2511S In distribution
MDL2511L In distribution
MDL2510 In distribution
MDL2513L In distribution
MDL2015S In distribution
MDL2010 In distribution
MDL2011S In distribution
MDL2018S In distribution
MDL2511 In distribution
MDL2513S In distribution
MDL2018S In distribution
MDL2008S In distribution
MDL2515L In distribution
MDL2518A Angle 15 ° In distribution
MDL2518 In distribution
MDL2510L In distribution
MDL2008 In distribution
MDL2018 In distribution
MDL2011S In distribution
MDL2015 In distribution
MDL2013S In distribution
MDL2010S In distribution
MDL2510S In distribution
MDL2010 In distribution
MDL2515S In distribution
MDL2513A Angle 15 ° In distribution
MDL2008S In distribution
MDL2013 In distribution
MDL2013P In distribution
MDLOP2518 Withdrawn
MDLOP2515 Withdrawn
MDL2011S Withdrawn
MDLOP2513 Withdrawn

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
K133613 2014-03-20
K130140 2013-08-01
K103194 2011-04-21
K070601 2007-10-12
K050970 2005-10-14
K031322 2003-12-23
K021915 2002-12-19
K021322 2002-07-24

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