SimpliCore

Kerr SimpliCore Obturator for ZenFlex ONE Size Primary - 20PK

Registry build 21.09.26
42manufacturers in China registered for this device type
33catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Guangdong (9), Shanghai (8), Jiangsu (6). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EKM
Manufacturer City Province Registered as Device types
Shenzhen Denco Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 52
Hantech Medical Device Co., Ltd. Cixi Zhejiang Contract manufacturer 18
Dentsply Dental (Tianjin) Co., Ltd. Teda Tianjin Contract manufacturer 2
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Shanghai Jolly Industrial Co., Ltd. Shanghai Shanghai Contract manufacturer 99
Shanghai Lions Industrial Co., Ltd. Shanghai Shanghai Contract manufacturer 82
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66
Hubei Guarddent Medical Technology Co., Ltd. Wuhan Hubei Manufacturer 60
Tribest Dental Products Co Ltd Yangzhong Jiangsu Contract manufacturer 58
Shenzhen Rogin Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 51
Anqing Clean Dental Instrument Technology Co., Ltd. Anqing Anhui Manufacturer 50
Shanghai Dochem Industries Co., Ltd. Shanghai Shanghai Manufacturer 45

Showing 12 of 42. All 42 manufacturers in China registered for Gutta-Percha

Record

Regulatory record for SimpliCore
Listed by Kerr Corporation, United States
FDA product code EKM
Device type Gutta-Percha
Device class Class 1
Regulation 21 CFR 872.3850
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2026-02-10

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Liquid Chemical
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: 10° C – 37.8° C

Catalogue Numbers

Catalogue numbers for SimpliCore
Catalogue number Size Per pack Status
972-3420 20 In distribution
972-3430 20 In distribution
818-2614 6 In distribution
818-2613 6 In distribution
972-3825 6 In distribution
972-3340 6 In distribution
818-2616 6 In distribution
825-9551 6 In distribution
972-3335 6 In distribution
818-2617 20 In distribution
825-9550 6 In distribution
825-9553 6 In distribution
972-3835 6 In distribution
972-3840 6 In distribution
818-2620 20 In distribution
972-3330 6 In distribution
818-2615 6 In distribution
972-3350 6 In distribution
818-2618 20 In distribution
818-2619 20 In distribution
972-3345 6 In distribution
972-3830 6 In distribution
972-3320 6 In distribution
972-3435 20 In distribution
972-3820 6 In distribution
825-9552 6 In distribution
972-3440 20 In distribution
972-3850 6 In distribution
972-3845 6 In distribution
972-3325 6 In distribution
972-3445 20 In distribution
972-3425 20 In distribution
972-3450 20 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Gutta Percha Points Diadent Group Intl., Inc. 1,404
MM Marked Gutta Percha Points Diadent Group Intl., Inc. 683
Henry Schein Henry Schein, Inc. 386
Zarc Shanghai Xing YU Medical Equipment Co., Ltd. 166
Darby Dental Supply, LLC Darby Dental Supply, LLC 130
Brasseler USA Peter Brasseler Holdings, LLC 126
Avalon Biomed Shanghai Xing YU Medical Equipment Co., Ltd. 106
Advance Dental Products THE Atlanta Dental Supply Company 97
Safco gutta percha points Safco Dental Supply 90
Sure-endo Sure Dent Corporation 89
3D Endo 3D Dental Designs AND Development, LLC 82
Endodontic Obturators Tulsa Dental Products LLC 78

Showing 12 of 599. All products under Gutta-Percha

Recalls

The FDA has not published a severity grade for these. 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
2009-10-27 Not classified Component design/selection The recall was initiated because during the manufacturing process of the affected units, the molding process resulted in lock nuts that did not have the level of acceptability required, and therefore, may not withstand the pressures exhibit 5046 units (3720 units in US) 2012-03-22

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