Edge Sequel Sapphire

90 catalogue numbers from ES500421, listed by US Endodontics, LLC, United States, under File, Pulp Canal, Endodontic. 53 manufacturers in China are registered for this product code.

Registry build 21.09.26
53manufacturers in China registered for this device type
90catalogue numbers in this listing
1recall

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 Edge Sequel Sapphire
Listed by US Endodontics, LLC, United States
FDA product code EKS
Device type File, Pulp Canal, Endodontic
Device class Class 1
Regulation 21 CFR 872.4565
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2023-04-25

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Edge Sequel Sapphire
Catalogue number Size Per pack Status
ES500421 4 In distribution
ES800431 4 In distribution
ESSAST0421 4 In distribution
ESSAST0625L 4 In distribution
ES300425 4 In distribution
ES550421 4 In distribution
ES200631 4 In distribution
ES350621 4 In distribution
ES250425 4 In distribution
ASST35500425 4 In distribution
ASST15300631 4 In distribution
ES800421 4 In distribution
ES250621 4 In distribution
ES250631 4 In distribution
ES900431 4 In distribution
ES400431 4 In distribution
ES400425 4 In distribution
ES200425 4 In distribution
ASST15300621 4 In distribution
ASST15300625 4 In distribution
ES600425 4 In distribution
ES600431 4 In distribution
ES800425 4 In distribution
ES450625 4 In distribution
ESSAST0621 4 In distribution
ESSAST0631 4 In distribution
ES700431 4 In distribution
ES350421 4 In distribution
ES300621 4 In distribution
ES350425 4 In distribution
ES450425 4 In distribution
ESSAST0631L 4 In distribution
ASST35500621 4 In distribution
ES250821 4 In distribution
ES500425 4 In distribution
ES400631 4 In distribution
ES200431 4 In distribution
ASST35500431 4 In distribution
ES250431 4 In distribution
ES500625 4 In distribution
ES250421 4 In distribution
ASST35500421 4 In distribution
ESSAST0431 4 In distribution
ES550431 4 In distribution
ES300625 4 In distribution
ASST15300421 4 In distribution
ESSAST0621L 4 In distribution
ESSAST0425 4 In distribution
ES450421 4 In distribution
ES200621 4 In distribution
ES350625 4 In distribution
ES150425 4 In distribution
ES400421 4 In distribution
ES900425 4 In distribution
ES350431 4 In distribution
ES200625 4 In distribution
ES300631 4 In distribution
ES200421 4 In distribution
ES500631 4 In distribution
ES450631 4 In distribution
ES400625 4 In distribution
ES700421 4 In distribution
ESSAST0431L 4 In distribution
ESSAST0425L 4 In distribution
ES450431 4 In distribution
ES150431 4 In distribution
ES400621 4 In distribution
ES150621 4 In distribution
ES700425 4 In distribution
ES350631 4 In distribution
ES250825 4 In distribution
ES500431 4 In distribution
ES250831 4 In distribution
ASST15300431 4 In distribution
ES150631 4 In distribution
ESSAST0421L 4 In distribution
ESSAST0625 4 In distribution
ES150421 4 In distribution
ASST35500631 4 In distribution
ASST15300425 4 In distribution
ES300431 4 In distribution
ES450621 4 In distribution
ES250625 4 In distribution
ES150625 4 In distribution
ES300421 4 In distribution
ES500621 4 In distribution
ES550425 4 In distribution
ES900421 4 In distribution
ASST35500625 4 In distribution
ES600421 4 In distribution

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

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
2025-01-02 Class II Under Investigation by firm Due to devices being irradiated above the established specification which my result in package integrity issues. Total devices=789,729 (47,508 devices (U.S.) and 742,221 dev

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