S-Clean Tapered II Fixture

Dental Implant System / s-Clean tapered II Fixture Set (Fixture + Cover Screw)

Registry build 21.09.26
7manufacturers in China registered for this device type
48catalogue numbers in this listing
19510(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 s-Clean tapered II Fixture
Listed by Dentis Co., Ltd., South Korea
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Manufacturer, Exporter
Record published 2019-06-07
Record revised 2021-05-26 (version 6)

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

Catalogue Numbers

Catalogue numbers for s-Clean tapered II Fixture
Catalogue number Size Status
DS2FR4114S In distribution
DS2FW4812 In distribution
DS2FW4809S In distribution
DS2FR4108 In distribution
DS2FR4312S In distribution
DS2FR4109 In distribution
DS2FM3714S In distribution
DS2FW4814S In distribution
DS2FR4307 In distribution
DS2FW4812S In distribution
DS2FW4807S In distribution
DS2FW4808 In distribution
DS2FR4109S In distribution
DS2FR4309S In distribution
DS2FR4107 In distribution
DS2FR4114 In distribution
DS2FR4308S In distribution
DS2FM3714 In distribution
DS2FW4809 In distribution
DS2FM3707S In distribution
DS2FR4314 In distribution
DS2FM3708 In distribution
DS2FM3708S In distribution
DS2FR4307S In distribution
DS2FM3710 In distribution
DS2FR4110S In distribution
DS2FW4810 In distribution
DS2FW4807 In distribution
DS2FR4314S In distribution
DS2FW4808S In distribution
DS2FR4312 In distribution
DS2FR4310 In distribution
DS2FR4110 In distribution
DS2FM3707 In distribution
DS2FM3710S In distribution
DS2FM3712 In distribution
DS2FR4112 In distribution
DS2FR4308 In distribution
DS2FM3709S In distribution
DS2FR4108S In distribution
DS2FR4309 In distribution
DS2FW4810S In distribution
DS2FM3712S In distribution
DS2FM3709 In distribution
DS2FR4112S In distribution
DS2FW4814 In distribution
DS2FR4107S In distribution
DS2FR4310S 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
K253493 2026-03-04
K240511 2024-05-20
K210080 2021-06-04
K210134 2021-04-19
K202773 2021-03-18
K210132 2021-02-17
K200099 2020-04-13
K192688 2020-02-04
K171027 2017-09-06
K170220 2017-04-27
K161244 2016-12-07
K160213 2016-06-21
K153639 2016-04-08
K142313 2015-12-10
K150344 2015-07-24
K111364 2012-02-01
K082843 2009-06-19
K083586 2009-04-29
K073486 2008-04-04

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