EK III NH Fixture Pre-Mounted

58 catalogue numbers from AEK3S5008B, listed by Hiossen Inc., United States, 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
58catalogue numbers in this listing
15510(k) clearances naming this product code
1recall

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 EK III NH Fixture Pre-Mounted
Listed by Hiossen Inc., United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K203360
Record published 2022-01-13
Record revised 2024-09-18 (version 3)

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, serial number
Distribution end date 2024-09-17

Catalogue Numbers

Catalogue numbers for EK III NH Fixture Pre-Mounted
Catalogue number Size Status
AEK3S5008B In distribution
AEK3S6013B In distribution
AEK3S4507B In distribution
AEK3S3513B In distribution
AEK3S3008B In distribution
AEK3S5508B In distribution
AEK3S7008B In distribution
AEK3S5511B In distribution
AEK3S4508B In distribution
AEK3S4007B In distribution
AEK3S3013B In distribution
AEK3S4013B In distribution
AEK3S5010B In distribution
AEK3S7010B In distribution
AEK3S4010B In distribution
AEK3S4008B In distribution
AEK3S5507B In distribution
AEK3S4510B In distribution
AEK3S3011B In distribution
AEK3S6010B In distribution
AEK3S6008B In distribution
AEK3S5513B In distribution
AEK3S7007B In distribution
AEK3S5013B In distribution
AEK3S7011B In distribution
AEK3S3511B In distribution
AEK3S6011B In distribution
AEK3S6007B In distribution
AEK3S5510B In distribution
AEK3S6006B In distribution
AEK3S3010B In distribution
AEK3S5011B In distribution
AEK3S7013B In distribution
AEK3S5007B In distribution
AEK3S4011B In distribution
AEK3S4513B In distribution
AEK3S4511B In distribution
AEK3S3510B In distribution
AEK3S3508B In distribution
AEK3S3007B In distribution
AEK3S7006B In distribution
AEK3S3013B Withdrawn
AEK3S7006B Withdrawn
AEK3S6010B Withdrawn
AEK3S6007B Withdrawn
AEK3S3007B Withdrawn
AEK3S7007B Withdrawn
AEK3S6011B Withdrawn
AEK3S3008B Withdrawn
AEK3S6013B Withdrawn
AEK3S6006B Withdrawn
AEK3S6008B Withdrawn
AEK3S7011B Withdrawn
AEK3S3011B Withdrawn
AEK3S7010B Withdrawn
AEK3S7008B Withdrawn
AEK3S3010B Withdrawn
AEK3S7013B 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
K240232 2024-09-13
K203360 2022-01-07
K191751 2019-12-16
K191201 2019-11-15
K183242 2019-05-21
K153332 2016-10-27
K151626 2016-07-21
K140934 2014-11-12
K123471 2013-07-05
K112532 2012-08-06
K103537 2011-03-10
K101096 2010-10-08
K093889 2010-04-22
K093352 2009-11-24
K090237 2009-04-17

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2023-04-06 Class II Labeling Change Control Mis-labeled length of the dental implant on the Recall Implant’s package. Dental implant size D5.0 x L8.5mm, labeled as D5.0 x L10mm 287 units

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