Admira Fusion

Universal nanohybrid ORMOCER restorative material. This kit contains different shades of Admira Fusion, Admira Fusion x-tra and Futurabond U.

Registry build 21.09.26
10manufacturers in China registered for this device type
46catalogue numbers in this listing
45510(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 Admira Fusion
Listed by Voco Gmbh, Germany
FDA product code EBF
Device type Material, Tooth Shade, Resin
Device class Class 2
Regulation 21 CFR 872.3690
Establishment Specification developer, Repacker / relabeller, Private-label distributor, Manufacturer, Exporter
510(k) K150784
Record published 2016-08-31
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 4 to 23 °C

Catalogue Numbers

Catalogue numbers for Admira Fusion
Catalogue number Size Per pack Status
2801 15 In distribution
2788 15 In distribution
2809 15 In distribution
2775 In distribution
2790 15 In distribution
2782 15 In distribution
2796 15 In distribution
2798 15 In distribution
2759 In distribution
2760 In distribution
2758 In distribution
2754 In distribution
2764 In distribution
2752 In distribution
2792 15 In distribution
2750 In distribution
2770 In distribution
2794 15 In distribution
2768 In distribution
2804 15 In distribution
2800 15 In distribution
2751 5 In distribution
2805 15 In distribution
2773 In distribution
2803 15 In distribution
2791 15 In distribution
2784 15 In distribution
2755 In distribution
2777 In distribution
2763 In distribution
2785 15 In distribution
2786 15 In distribution
2781 75 In distribution
2762 In distribution
2757 In distribution
2787 15 In distribution
2779 15 In distribution
2806 15 In distribution
2756 In distribution
2772 In distribution
2771 In distribution
2778 In distribution
2776 In distribution
2766 In distribution
2799 15 In distribution
2783 15 In distribution

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
K261357 2026-04-27
K251239 2025-05-21
K230877 2023-07-13
K201307 2020-07-08
K200294 2020-03-27
K190453 2019-04-11
K181312 2018-08-22
K171815 2017-11-15
K171200 2017-08-10
K170896 2017-06-29
K153493 2016-07-29
K153177 2016-06-30
K151956 2015-10-20
K150784 2015-07-02
K123773 2012-12-21
K113444 2011-12-21
K113563 2011-12-21
K112447 2011-11-08
K112374 2011-10-20
K110589 2011-05-27
K103580 2011-01-21
K102354 2010-11-08
K102351 2010-11-02
K102450 2010-10-08
K101213 2010-08-19
K090843 2009-06-17
K071386 2007-06-05
K063604 2007-01-22
K062345 2006-12-15
K062343 2006-11-02
K060893 2006-05-25
K053391 2006-02-15
K051867 2005-07-27
K051868 2005-07-27
K033117 2003-11-25
K030914 2003-05-30
K030915 2003-05-30
K022797 2002-10-10
K014111 2002-03-06
K011756 2001-07-18
K994304 2000-02-07
K994268 2000-02-03
K994056 2000-01-12
K926418 1993-03-31
K920365 1992-03-19

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
2019-07-09 Class II Process control The metal cannula are potentially too loose and may become loose when applying the filing material. 5 units 2023-04-20

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