US/SS/GS System

47 catalogue numbers from BFM213A, listed by Osstem Implant Co., Ltd., South Korea, under Implant, Endosseous, Root-Form. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
47catalogue numbers in this listing
27510(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 US/SS/GS System
Listed by Osstem Implant Co., Ltd., South Korea
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Contract manufacturer, Specification developer, Private-label distributor, Complaint-file establishment, Manufacturer, Exporter
510(k) K073247
Record published 2022-11-28
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for US/SS/GS System
Catalogue number Size Status
BFM213A In distribution
ABFR313A In distribution
AUS3R415AR In distribution
ABFR308A In distribution
AUS3W510AR In distribution
AUS3R411AR In distribution
AUS3R408AR In distribution
ABFR307A In distribution
AUS3W508AR In distribution
AUS3W613AR In distribution
ABFM213A In distribution
ABFM210A In distribution
ABFW510A In distribution
ABFM208A In distribution
ABFW507A In distribution
AUS3R410AR In distribution
ABFW610A In distribution
ABFR410A In distribution
ABFM215A In distribution
ABFR311A In distribution
ABFR413A In distribution
ABFW607A In distribution
ABFW608A In distribution
ABFM211A In distribution
AUS3W515AR In distribution
ABFW511A In distribution
ABFR411A In distribution
AUS3W611AR In distribution
AUS3W513AR In distribution
ABFR315A In distribution
AUS3W615AR In distribution
ABFW613A In distribution
AUS3W511AR In distribution
ABFR407A In distribution
ABFW515A In distribution
ABFR310A In distribution
AUS3R413AR In distribution
ABFW513A In distribution
BFM208A In distribution
ABFR415A In distribution
ABFW611A In distribution
ABFR408A In distribution
ABFW615A In distribution
ABFW508A In distribution
SSPSN600TH In distribution
AUS3W608AR In distribution
SSPSO600TH 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
K222778 2023-09-23
K163557 2017-05-15
K163088 2017-04-21
K161103 2017-02-02
K161604 2016-10-17
K121585 2013-01-07
K121995 2012-11-29
K122171 2012-11-16
K120847 2012-08-10
K091208 2010-03-03
K091678 2010-02-18
K083633 2009-05-01
K083067 2009-02-02
K082213 2008-10-14
K080594 2008-09-03
K080744 2008-07-17
K081078 2008-07-15
K073465 2008-04-07
K080387 2008-03-07
K073247 2008-03-07
K072959 2008-02-04
K072871 2008-01-10
K072896 2007-11-06
K063861 2007-09-21
K062030 2006-11-02
K062051 2006-11-01
K062156 2006-10-20

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