MasterSeries

DB Bracket Master Series Mand Right 1ST Bicuspid Offset 022 TQ=-12 A=+2 R=0 Hook D-G PROFILE=072 HGW M/D=120 O/G=115 System=mbt

Registry build 21.09.26
52manufacturers in China registered for this device type
45catalogue numbers in this listing
22510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (19), Guangdong (11), Jiangsu (9). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EJF
Manufacturer City Province Registered as Device types
Shenzhen Denco Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 52
Sino Ortho Limited Hangzhou Zhejiang Contract manufacturer 14
Hangzhou Westlake Biomaterial Co., Ltd. Hangzhou Zhejiang Contract manufacturer 13
Chengdu Sani Medical Equipment Co., Ltd. Chengdu Sichuan Contract manufacturer 12
Hangzhou Xingchen 3B Dental Instrument & Materials Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Yancheng Denrum Medical Apparatus Co., Ltd. Yancheng Jiangsu Contract manufacturer 5
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66
Shanghai MU Promotions Co., Ltd. Shanghai Shanghai Exporter 62
Guangzhou Four E’s Scientific Co., Ltd. Guangzhou Guangdong Contract manufacturer 61
Hubei Guarddent Medical Technology Co., Ltd. Wuhan Hubei Manufacturer 60
Tribest Dental Products Co Ltd Yangzhong Jiangsu Contract manufacturer 58

Showing 12 of 52. All 52 manufacturers in China registered for Bracket, Metal, Orthodontic

Record

Regulatory record for MasterSeries
Listed by American Orthodontics, United States
FDA product code EJF
Device type Bracket, Metal, Orthodontic
Device class Class 1
Regulation 21 CFR 872.5410
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2018-08-03
Record revised 2025-06-27 (version 7)

Specifications

Specifications
MRI safety MR Unsafe
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Distribution end date 2025-06-26

Catalogue Numbers

Catalogue numbers for MasterSeries
Catalogue number Size Status
390-8507B In distribution
390-0115HD In distribution
390-0114HD In distribution
390-0115B In distribution
390-0008 In distribution
970-0104B In distribution
970-0056B In distribution
390-8809B In distribution
970-0115HD In distribution
310-0114B In distribution
390-0404 In distribution
390-0114B In distribution
970-0105B In distribution
390-0028 In distribution
390-8829B In distribution
970-0115B In distribution
390-0504 In distribution
390-0104HD In distribution
970-0114B In distribution
970-0114HD In distribution
390-0056B In distribution
390-8063B In distribution
390-0504B In distribution
390-0503B In distribution
390-0105HD In distribution
390-0403 In distribution
390-8828B In distribution
390-0016 In distribution
390-8072B In distribution
390-0105B In distribution
390-8508B In distribution
390-0104B In distribution
390-0503 In distribution
390-8808B In distribution
390-0021M Withdrawn
390-0021PM Withdrawn
390-0322 Withdrawn
390-8712B Withdrawn
390-8716B Withdrawn
390-0404B Withdrawn
390-0021PD Withdrawn
390-8717B Withdrawn
390-0021D Withdrawn
390-8713B Withdrawn
390-0403B Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Leone SPA Leone SPA 2,306
BioQuick® Forestadent Bernhard Förster GmbH 1,842
Mini Master Series American Orthodontics 1,505
Mini-Mono® Forestadent Bernhard Förster GmbH 1,225
LP Low Profile American Orthodontics 1,204
Mini Sprint® Forestadent Bernhard Förster GmbH 1,193
Empower Bracket American Orthodontics 1,175
Legend GC Orthodontics America Inc. 1,098
Master Series American Orthodontics 1,084
Experience® GC Orthodontics America Inc. 770
The Orthodontic Store Young Innovations Inc. 658
equilibrium® Dentaurum GmbH & Co. KG 646

Showing 12 of 876. All products under Bracket, Metal, Orthodontic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K925012 1993-09-13
K923261 1992-12-03
K902064 1990-08-06
K900488 1990-06-01
K891331 1989-10-16
K893482 1989-10-12
K893655 1989-08-23
K893483 1989-07-14
K893555 1989-07-14
K893550 1989-07-14
K893484 1989-07-14
K893654 1989-06-23
K893549 1989-06-23
K893542 1989-06-23
K891775 1989-05-11
K891599 1989-05-02
K890536 1989-05-01
K890656 1989-04-17
K891484 1989-04-14
K891592 1989-04-07
K890581 1989-03-17
K890145 1989-03-13

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