K-File Nitiflex

Root Canal File

Registry build 21.09.26
53manufacturers in China registered for this device type
22catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (13), Jiangsu (8), Shanghai (7). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EKS
Manufacturer City Province Registered as Device types
Shenzhen Denco Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 52
Shenzhen Rogin Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 51
Suzhou Pac-Dent Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 26
Denjoy Dental Co., Ltd. Changsha Hunan Contract manufacturer 17
Sino Ortho Limited Hangzhou Zhejiang Contract manufacturer 14
Shenzhen Superline Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 12
Wuhu Guli Ortho Co., Ltd. Wuhu Anhui Contract manufacturer 12
Shenzhen Forever Medical Devices Co., Ltd. Shenzhen Guangdong Contract manufacturer 9
Zhejiang Eksen Medical Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 9
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Zogear Medical Co., Ltd. Yizheng Jiangsu Contract manufacturer 75
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66

Showing 12 of 53. All 53 manufacturers in China registered for File, Pulp Canal, Endodontic

Record

Regulatory record for K-File Nitiflex
Listed by Maillefer Instruments Holding Sàrl
FDA product code EKS
Device type File, Pulp Canal, Endodontic
Device class Class 1
Regulation 21 CFR 872.4565
Premarket notification Exempt
Record published 2022-09-30
Record revised 2025-06-06 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number
Storage Special storage condition: N/A
Distribution end date 2023-06-30

Catalogue Numbers

Catalogue numbers for K-File Nitiflex
Catalogue number Size Status
A012N02505512 Withdrawn
A012N02104012 Withdrawn
A012N02502512 Withdrawn
A012N02102012 Withdrawn
A012N02102512 Withdrawn
A012N02101512 Withdrawn
A012N02504012 Withdrawn
A012N02590012 Withdrawn
A012N02505012 Withdrawn
A012N02501512 Withdrawn
A012N02503012 Withdrawn
A012N02506012 Withdrawn
A012N02503512 Withdrawn
A012N02104512 Withdrawn
A012N02502012 Withdrawn
A012N02103012 Withdrawn
A012N02106012 Withdrawn
A012N02504512 Withdrawn
A012N02105012 Withdrawn
A012N02103512 Withdrawn
A012N02190012 Withdrawn
A012N02105512 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Henry Schein Henry Schein, Inc. 720
Integra® Miltex® Integra LifeSciences Production Corporation 658
Endodontic Hand Instruments Tulsa Dental Products LLC 612
Brasseler USA Peter Brasseler Holdings, LLC 526
Darby Dental Supply, LLC Darby Dental Supply, LLC 456
3D Endo 3D Dental Designs AND Development, LLC 283
Avalon Biomed Shenzhen Denco Medical Co., Ltd. 233
KP Guilin Kevin Peter Technology Co., Ltd. 216
Dctaper SS White Burs LLC 205
Advance Dental Products THE Atlanta Dental Supply Company 205
Edge File US Endodontics, LLC 202
Komet Root Canal Files Gebr. Brasseler Gmbh & Co. KG 199

Showing 12 of 1,536. All products under File, Pulp Canal, Endodontic

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