DS PrimeTaper

PrimeTaper EV Ø5.4 x 6.5mm OsseoSpeed

Registry build 21.09.26
7manufacturers in China registered for this device type
59catalogue numbers in this listing
1510(k) clearance

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 DS PrimeTaper
Listed by Dentsply Implants Manufacturing GmbH, Germany
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Contract manufacturer, Manufacturer
Record published 2023-02-08
Record revised 2023-08-30 (version 4)

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
Distribution end date 2023-08-30
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for DS PrimeTaper
Catalogue number Size Status
68011098 In distribution
68011110 In distribution
68011100 In distribution
68011107 In distribution
68011093 In distribution
68011096 In distribution
68011104 In distribution
68011091 In distribution
68011113 In distribution
68011112 In distribution
68011087 In distribution
68011106 In distribution
68011090 In distribution
68011105 In distribution
68011101 In distribution
68011088 In distribution
68011086 In distribution
68011111 In distribution
68011109 In distribution
68011102 In distribution
68011092 In distribution
68011089 In distribution
68011103 In distribution
68011108 In distribution
68011099 In distribution
68011097 In distribution
68011095 In distribution
68011085 In distribution
68011114 In distribution
68011115 In distribution
68011094 In distribution
68011115 Withdrawn
68011086 Withdrawn
68011107 Withdrawn
68011095 Withdrawn
68011110 Withdrawn
68011097 Withdrawn
68011103 Withdrawn
68011113 Withdrawn
68011104 Withdrawn
68011096 Withdrawn
68011089 Withdrawn
68011101 Withdrawn
68011098 Withdrawn
68011102 Withdrawn
68011093 Withdrawn
68011106 Withdrawn
68011088 Withdrawn
68011100 Withdrawn
68011085 Withdrawn
68011108 Withdrawn
68011109 Withdrawn
68011111 Withdrawn
68011114 Withdrawn
68011105 Withdrawn
68011094 Withdrawn
68011112 Withdrawn
68011087 Withdrawn
68011099 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
K130999 2013-10-25

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