Camlog® Screw-Line Implant, Promote®

K1045.5011 CAMLOG® SCREW-LINE Implant, Promote®, screw-mounted, d 5.0, L 11

Registry build 21.09.26
7manufacturers in China registered for this device type
71catalogue numbers in this listing
5510(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 Camlog® Screw-Line Implant, Promote®
Listed by Altatec Gmbh, Germany
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Manufacturer
Record published 2020-10-12
Record revised 2023-06-16 (version 3)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Length 9 to 16 mm; outer diameter 3.3 to 6 mm; lumen/inner diameter 3.3 to 6 mm
Distribution end date 2025-04-03

Catalogue Numbers

Catalogue numbers for Camlog® Screw-Line Implant, Promote®
Catalogue number Size Status
K1046.3311 Outer Diameter 3.3 mm In distribution
K1045.5011 Outer Diameter 5.0 mm In distribution
K1046.5009 Outer Diameter 5.0 mm In distribution
K1046.5016 Outer Diameter 5.0 mm In distribution
K1046.3811 Outer Diameter 3.8 mm In distribution
K1045.5013 Outer Diameter 5.0 mm In distribution
K1045.3313 Outer Diameter 3.3 mm In distribution
K1045.4309 Outer Diameter 4.3 mm In distribution
K1046.6011 Outer Diameter 6.0 mm In distribution
K1046.3313 Outer Diameter 3.3 mm In distribution
K1045.5009 Outer Diameter 5.0 mm In distribution
K1045.3811 Outer Diameter 3.8 mm In distribution
K1045.3311 Outer Diameter 3.3 mm In distribution
K1046.6016 Outer Diameter 6.0 mm In distribution
K1045.4316 Outer Diameter 4.3 mm In distribution
K1046.4313 Outer Diameter 4.3 mm In distribution
K1042.3313 Length 13 mm In distribution
K1046.3816 Outer Diameter 3.8 mm In distribution
K1046.5013 Outer Diameter 5.0 mm In distribution
K1046.4316 Outer Diameter 4.3 mm In distribution
K1046.6009 Outer Diameter 6.0 mm In distribution
K1046.4309 Outer Diameter 4.3 mm In distribution
K1045.3813 Outer Diameter 3.8 mm In distribution
K1046.4311 Outer Diameter 4.3 mm In distribution
K1045.3816 Outer Diameter 3.8 mm In distribution
K1046.6013 Outer Diameter 6.0 mm In distribution
K1046.5011 Outer Diameter 5.0 mm In distribution
K1045.4313 Outer Diameter 4.3 mm In distribution
K1044.3313 Outer Diameter 3.3 mm In distribution
K1045.3809 Outer Diameter 3.8 mm In distribution
K1045.3316 Outer Diameter 3.3 mm In distribution
K1046.3813 Outer Diameter 3.8 mm In distribution
K1046.3809 Outer Diameter 3.8 mm In distribution
K1046.3316 Outer Diameter 3.3 mm In distribution
K1045.4311 Outer Diameter 4.3 mm In distribution
K1044.4316 Length 16 mm Withdrawn
K1044.3316 Length 16 mm Withdrawn
K1042.6016 Lumen/Inner Diameter 6.0 mm Withdrawn
K1044.4309 Length 9 mm Withdrawn
K1042.3311 Length 11 mm Withdrawn
K1044.6013 Length 13 mm Withdrawn
K1042.6013 Lumen/Inner Diameter 6.0 mm Withdrawn
K1044.5009 Length 9 mm Withdrawn
K1042.3316 Lumen/Inner Diameter 3.3 mm Withdrawn
K1044.5016 Length 16 mm Withdrawn
K1044.3813 Length 13 mm Withdrawn
K1044.5011 Length 11 mm Withdrawn
K1042.5016 Outer Diameter 5.0 mm Withdrawn
K1044.4311 Length 11 mm Withdrawn
K1044.4313 Length 13 mm Withdrawn
K1042.3811 Lumen/Inner Diameter 3.8 mm Withdrawn
K1042.4311 Lumen/Inner Diameter 4.3 mm Withdrawn
K1044.3809 Length 9 mm Withdrawn
K1044.6016 Length 16 mm Withdrawn
K1042.5013 Lumen/Inner Diameter 5.0 mm Withdrawn
K1042.3813 Lumen/Inner Diameter 3.8 mm Withdrawn
K1042.4309 Outer Diameter 4.3 mm Withdrawn
K1044.5013 Length 13 mm Withdrawn
K1044.6011 Length 11 mm Withdrawn
K1042.4316 Lumen/Inner Diameter 4.3 mm Withdrawn
K1042.6009 Lumen/Inner Diameter 6.0 mm Withdrawn
K1042.6011 Lumen/Inner Diameter 6.0 mm Withdrawn
K1042.3816 Lumen/Inner Diameter 3.8 mm Withdrawn
K1042.5009 Lumen/Inner Diameter 5.0 mm Withdrawn
K1042.5011 Lumen/Inner Diameter 5.0 mm Withdrawn
K1044.3816 Length 16 mm Withdrawn
K1044.3811 Length 11 mm Withdrawn
K1042.3809 Lumen/Inner Diameter 3.8 mm Withdrawn
K1042.4313 Lumen/Inner Diameter 4.3 mm Withdrawn
K1044.3311 Outer Diameter 3.3 mm Withdrawn
K1044.6009 Length 9 mm 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
K193401 2020-09-29
K151599 2015-10-02
K133991 2014-08-06
K113779 2012-12-14
K083496 2009-01-30

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