Quad Key

Quad Key Composite

Registry build 21.09.26
64manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Guangdong (17), Jiangsu (10), Hebei (5). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZN
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
BH Medical Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 37
Shenzhen Senlede Technologies Co., Ltd. Shenzhen Guangdong Contract manufacturer 33
Suzhou Pac-Dent Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 26
iBrite Suzhou Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 18
Acot Plastics (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 8
medmix China Ltd Shanghai Shanghai Contract manufacturer 2
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Shanghai Jolly Industrial Co., Ltd. Shanghai Shanghai Contract manufacturer 99

Showing 12 of 64. All 64 manufacturers in China registered for Instruments, Dental Hand

Record

Regulatory record for Quad Key
Listed by Ultradent Products Inc., United States
FDA product code DZN
Device type Instruments, Dental Hand
Device class Class 1
Regulation 21 CFR 872.4565
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2018-08-31

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Quad Key
Catalogue number Size Status
3080- In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LMDental LM-Dental 936
A. Titan Instruments A. Titan Instruments, Inc. 544
Instruments, Dental Hand Hager & Meisinger Gesellschaft mit beschränkter Haftung 307
Power Dental USA Power Dental U.S.A. Inc. 209
Supremo Instrumentos Andre Gregate Braga Instrumentos Ltda 95
Henry Schein Henry Schein, Inc. 93
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 92
Diamodent Diamodent 81
Stoma® Storz AM Mark Gmbh 80
Nordent Manufacturing Inc Nordent Manufacturing Inc 77
Brasseler USA Peter Brasseler Holdings, LLC 67
BMT Medizintechnik GmbH BMT Medizintechnik GmbH 58

Showing 12 of 1,362. All products under Instruments, Dental Hand

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 Closed
2015-12-22 Class II Nonconforming Material/Component Ultradent is recalling InterGuard 5.5mm Econo Refill, lot#s BC2GN and BC4L7 because product was received from the supplier with the floss tether hole not completely punched through and were distributed. 157 2016-10-19

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