Paradigm™

3M™ ESPE™ Paradigm™ MZ100 Blocks for CEREC™ System Refill, Shade A3.5, Size 14, 5 Blocks/Pack, 2714A3.5-S

Registry build 21.09.26
10manufacturers in China registered for this device type
49catalogue numbers in this listing
18510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangdong (3), Shandong (2), Jilin (2).

Chinese manufacturers registered for FDA product code EBF
Manufacturer City Province Registered as Device types
Aidite (Qinhuangdao) Technology Co., Ltd. Qinhuangdao Hebei Repacker / relabeller 17
Shandong Huge Dental Material Corporation Rizhao Shandong Manufacturer 17
Liaoning Upcera Co., Ltd. Benxi Liaoning Contract manufacturer 10
Shenzhen Upcera Digital Dental Technology Co., Ltd. Shenzhen Guangdong Exporter 10
Rizhao Huge Biomaterials Company, Ltd. Rizhao Shandong Manufacturer 7
Hangzhou SHINING3D Dental Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 7
Shenzhen Piocreat 3D Technology Co., Ltd. Shenzhen Guangdong Manufacturer 6
Shenzhen Upcera Dental Technology Co., Ltd. Shenzhen Guangdong Private-label distributor 6
Sincera Technology (Changchun) Co., Ltd. Changchun Jilin Manufacturer 2
Sino-Dentex Co., Ltd. Changchun Jilin Manufacturer 2

Record

Regulatory record for Paradigm™
Listed by 3M Company, United States
FDA product code EBF
Device type Material, Tooth Shade, Resin
Device class Class 2
Regulation 21 CFR 872.3690
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-24
Record revised 2023-02-23 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 10
Distribution end date 2021-06-30

Catalogue Numbers

Catalogue numbers for Paradigm™
Catalogue number Size Per pack Status
1481B1 20 In distribution
1480A4 In distribution
1480B1 In distribution
1481A4 20 In distribution
1481B2 20 In distribution
2714A1-S 5 In distribution
2714A2-S 5 In distribution
3714B3 5 In distribution
2714A3.5-S 5 In distribution
2714B3-S 5 In distribution
1481A1 20 In distribution
1481A3 20 In distribution
1481OA2 20 In distribution
3714A1 5 In distribution
1481OA3 20 In distribution
2714E-S 5 In distribution
1480OA3 In distribution
1480A2-S In distribution
1480A2 In distribution
1480A1 In distribution
3714A3.5 5 In distribution
3714E 5 In distribution
1481B3 20 In distribution
2714A3-S 5 In distribution
3714A3 5 In distribution
3714A2 5 In distribution
1480A3.5 In distribution
1481A3.5 20 In distribution
1481D3 20 In distribution
1480A3 In distribution
1480C2 In distribution
1480B3 In distribution
1481C2 20 In distribution
1480B2 In distribution
1481A2 20 In distribution
1480OA2 In distribution
1480D3 In distribution
2710A1-S 5 Withdrawn
3710A1 5 Withdrawn
3710A3.5 5 Withdrawn
3710A3 5 Withdrawn
2710E-S 5 Withdrawn
2710A3.5-S 5 Withdrawn
2710A2-S 5 Withdrawn
3710E 5 Withdrawn
2710A3-S 5 Withdrawn
3710A2 5 Withdrawn
2710B3-S 5 Withdrawn
3710B3 5 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Tooth Shade Resin Material Liaoning Upcera Co., Ltd. 4,808
Gradia® GC America Inc. 548
G-CAM Graphenano Dental, SL 320
Vitavm LC Vita – Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft 261
G-aenial™ GC America Inc. 225
Ena HRI ® Micerium SPA 221
Mazic Duro Vericom Co., Ltd. 206
Ceramage Shofu Dental Corp. 204
Filtek™ 3M Company 188
SR Nexco Ivoclar Vivadent Aktiengesellschaft 181
Aidite Aidite (Qinhuangdao) Technology Co., Ltd. 166
Tetric EvoCeram Ivoclar Vivadent Aktiengesellschaft 163

Showing 12 of 2,059. All products under Material, Tooth Shade, Resin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K163207 2016-11-28
K122569 2012-09-12
K100235 2010-05-12
K083610 2008-12-17
K072733 2008-02-15
K010781 2001-04-13
K991961 1999-08-09
K981647 1998-08-09
K970500 1997-04-30
K920425 1992-03-20
K872444 1987-09-11
K872279 1987-07-02
K861899 1986-06-25
K861740 1986-05-21
K851459 1985-05-21
K841550 1984-06-22
K833797 1984-04-25
K810595 1981-03-24

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
2015-06-15 Class II Device Design 3M is initiating a Field Correction to remove the crown indication from all Lava Ultimate products. These products will continue to be indicated for onlays, inlays and veneers. 1.8 million (US 1,017,834) 2016-04-26

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