Pure Ceramic Implants

RD Temporary Coping, for Bridge, PMMA

Registry build 21.09.26
15manufacturers in China registered for this device type
8catalogue numbers in this listing
47510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (11), Jiangsu (2), Shanghai (1). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NHA
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Modern Dental Laboratory (DG) Co., Ltd. Dongguan Guangdong Contract manufacturer 15
Exceldent Dental Technology Development Co., Ltd. Zhuhai Guangdong Contract manufacturer 12
DTS Digital Dental LAB Shenzhen Guangdong Contract manufacturer 11
KTJ Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Shimmer Computerized Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 10
Zhuhai Crystal Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 9
NEW Perfect Dental LAB Shenzhen Guangdong Contract manufacturer 8
Shenzhen Jiahong Dental Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 7
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
CBD Dental LAB, Inc Shenzhen Guangdong Manufacturer 11

Showing 12 of 15. All 15 manufacturers in China registered for Abutment, Implant, Dental, Endosseous

Record

Regulatory record for Pure Ceramic Implants
Listed by Institut Straumann AG, Switzerland
FDA product code NHA
Device type Abutment, Implant, Dental, Endosseous
Device class Class 2
Regulation 21 CFR 872.3630
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K151328
Record published 2016-01-14
Record revised 2019-09-02 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep away from sunlight
Sizes Outer diameter 3.3 to 4.1 mm

Catalogue Numbers

Catalogue numbers for Pure Ceramic Implants
Catalogue number Size Status
Protective caps Outer Diameter 4.1 mm In distribution
Protective caps Outer Diameter 4.1 mm In distribution
Protective caps AH 5.5mm In distribution
Temporary Coping Crown In distribution
Protective caps Outer Diameter 3.3 mm In distribution
Temporary Coping Outer Diameter 4.1 mm In distribution
Temporary Coping Bridge In distribution
Temporary Coping Bridge In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MEDENTiKA Medentika GmbH 2,553
LW Vis Abutment Ossvis Co., Ltd. 2,520
Dess dental smart solutions Terrats Medical SL 1,715
Locator Zest Anchors, LLC 1,643
NobelProcera® Nobel Biocare AB 1,526
Azure Terrats Medical SL 1,360
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 1,308
LW Vis Abutment SET Ossvis Co., Ltd. 1,260
Abutment, Implant, Dental, Endosseous Southern Implants (PTY) Ltd 1,240
Healing Abutment Megagen Implant Co., Ltd. 1,218
Chaorum Implant System Medimecca Co Ltd 1,084
OT Equator Rhein 83 SRL 1,051

Showing 12 of 6,204. All products under Abutment, Implant, Dental, Endosseous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260460 2026-05-07
K253315 2026-01-22
K243278 2025-02-21
K243478 2025-02-19
K222836 2023-05-15
K220878 2022-06-16
K220751 2022-06-02
K213063 2022-04-08
K203750 2021-10-09
K203456 2021-06-23
K201681 2021-03-18
K192742 2021-02-12
K203355 2021-02-12
K193046 2020-08-13
K192893 2020-01-03
K192029 2019-10-28
K190654 2019-06-28
K190097 2019-06-26
K190082 2019-04-17
K190040 2019-04-08
K173945 2018-10-05
K173968 2018-07-17
K173379 2018-03-30
K171649 2018-02-22
K172798 2018-01-03
K171773 2017-12-01
K162848 2017-09-22
K170354 2017-06-07
K170356 2017-06-07
K161677 2016-10-07
K120822 2012-12-21
K101465 2010-12-13
K091701 2009-12-22
K093113 2009-12-18
K082545 2008-10-17
K082764 2008-10-01
K081186 2008-05-23
K081005 2008-05-02
K072679 2007-10-12
K071357 2007-09-26
K072497 2007-09-26
K070549 2007-08-31
K072071 2007-08-15
K070744 2007-06-29
K051717 2005-07-07
K041295 2004-05-24
K040539 2004-03-18

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