Pure Ceramic Implants

Straumann® PURE Ceramic Implant Monotype, Ø 4.1mm RD, ZLA 10mm, AH 5.5mm, ZrO2

Registry build 21.09.26
7manufacturers in China registered for this device type
16catalogue numbers in this listing
31510(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 Pure Ceramic Implants
Listed by Institut Straumann AG, Switzerland
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K151328
Record published 2016-01-14
Record revised 2023-10-25 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep away from sunlight
Sizes Length 8 to 14 mm; outer diameter 3.3 to 4.1 mm

Catalogue Numbers

Catalogue numbers for Pure Ceramic Implants
Catalogue number Size Status
Ceramic TL Length 10 mm In distribution
Ceramic TL Outer Diameter 4.1 mm In distribution
Ceramic TL Length 8 mm In distribution
Ceramic TL AH 4mm In distribution
Ceramic TL Length 12 mm In distribution
Ceramic TL AH 5.5mm In distribution
Ceramic TL Length 10 mm In distribution
Ceramic TL Length 12 mm In distribution
Ceramic TL Length 8 mm In distribution
Ceramic TL Outer Diameter 4.1 mm In distribution
Ceramic TL Outer Diameter 3.3 mm In distribution
Ceramic TL AH 4mm In distribution
Ceramic TL Outer Diameter 3.3 mm In distribution
Ceramic TL Length 12 mm In distribution
Ceramic TL AH 4mm In distribution
Ceramic TL Outer Diameter 3.3 mm 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
K252168 2026-03-10
K250294 2025-08-12
K241391 2024-12-10
K234049 2024-03-20
K230108 2023-09-14
K223083 2023-06-22
K212533 2022-01-28
K211052 2021-07-08
K210855 2021-06-21
K200586 2020-08-20
K191256 2019-12-27
K191895 2019-12-09
K180477 2019-01-04
K181703 2018-12-28
K173961 2018-06-05
K153758 2016-03-23
K081419 2009-02-20
K062129 2006-10-20
K061176 2006-08-11
K053088 2006-02-27
K033984 2004-06-30
K033922 2004-01-07
K020096 2002-02-08
K013891 2002-02-05
K013798 2001-12-19
K003552 2001-08-17
K003271 2001-03-20
K983742 1999-03-15
K894595 1990-02-13
K894594 1990-02-13
K894593 1990-02-13

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