Forma S

Forma Global Compule Refill Trans/Incisal - 10 x 0.2g Capsules

Registry build 21.09.26
10manufacturers in China registered for this device type
44catalogue numbers in this listing
17510(k) clearances naming this product code
4recalls on this code

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 Forma S
Listed by Ultradent Products Inc., United States
FDA product code EBF
Device type Material, Tooth Shade, Resin
Device class Class 2
Regulation 21 CFR 872.3690
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
510(k) K240694
Record published 2024-08-14
Record revised 2025-08-21 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 27 °C

Catalogue Numbers

Catalogue numbers for Forma S
Catalogue number Size Status
5691 In distribution
5587 In distribution
5694 In distribution
5672 In distribution
5592 In distribution
5661 In distribution
5596 In distribution
5666 In distribution
5667 In distribution
5657 In distribution
5674 In distribution
5669 In distribution
S5696 In distribution
5642 In distribution
5653 In distribution
5660 In distribution
5585 In distribution
5692 In distribution
5588 In distribution
5693 In distribution
6027 In distribution
5586 In distribution
5677 In distribution
5688 In distribution
5686 In distribution
5659 In distribution
6029 In distribution
S5697 In distribution
5689 In distribution
5670 In distribution
5828 In distribution
5651 In distribution
5599 In distribution
5598 In distribution
5668 In distribution
5589 In distribution
5639 In distribution
5656 In distribution
6028 In distribution
5654 In distribution
6038 In distribution
5658 In distribution
5673 In distribution
5594 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
K262228 2026-07-01
K240694 2024-03-15
K221909 2022-07-01
K151094 2015-07-21
K043119 2004-12-17
K974413 1998-02-02
K974282 1998-01-29
K971898 1997-06-24
K965060 1997-01-31
K953525 1995-08-28
K950859 1995-03-23
K932227 1993-09-13
K931867 1993-09-09
K921598 1992-09-09
K921602 1992-09-09
K921407 1992-09-09
K921409 1992-09-09

Recalls

4 of these are 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
2024-08-02 Class II Material/Component Contamination Due to a manufacturing issue, red particulates present in the expressed composite. 560
2024-08-02 Class II Material/Component Contamination Due to a manufacturing issue, red particulates present in the expressed composite. 2450
2024-08-02 Class II Material/Component Contamination Due to a manufacturing issue, red particulates present in the expressed composite. 90
2020-08-31 Class II Under Investigation by firm Due to a potential manufacturing issue (cross contamination), composite is non-homogeneous. 412 syringes (206 kits) 2021-10-18

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