AuraVeneer Cement

AuraVeneer Cement. Kit of 4 x 1.2 ml Syringes. Shades: 1 Off White - 3 Opaque White

Registry build 21.09.26
3manufacturers in China registered for this device type
7catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (2), Guangdong (1).

Chinese manufacturers registered for FDA product code EMA
Manufacturer City Province Registered as Device types
Shandong Huge Dental Material Corporation Rizhao Shandong Manufacturer 17
Rizhao Huge Biomaterials Company, Ltd. Rizhao Shandong Manufacturer 7
Shenzhen Upcera Dental Technology Co., Ltd. Shenzhen Guangdong Private-label distributor 6

Record

Regulatory record for AuraVeneer Cement
Listed by Denali Corporation, United States
FDA product code EMA
Device type Cement, Dental
Device class Class 2
Regulation 21 CFR 872.3275
Record published 2016-08-04
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 4

Catalogue Numbers

Catalogue numbers for AuraVeneer Cement
Catalogue number Size Status
Clear In distribution
3 Clear – 1 Off White In distribution
1 Opaque White In distribution
1 Clear – 3 Off White In distribution
2 Clear – 2 Off-White In distribution
1 Off White – 3 Opaque White In distribution
Off White In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GC Fuji II LC® GC America Inc. 78
Equia® GC America Inc. 73
Riva SC SDI Ltd. 72
Denture Base American Tooth Industries 61
Riva LC SDI Ltd. 59
GC Fuji IX GP® GC America Inc. 58
GlasIonomer FX-LC Shofu Dental Corp. 45
Henry Schein Henry Schein, Inc. 35
Esthet-X®flow Liquid Micro Hybrid Dentsply LLC 24
Photac™ Fil Quick Aplicap™ 3M Deutschland GmbH 24
Ketac™ Fil Plus Aplicap™ 3M Deutschland GmbH 23
Ultra-Bond® DEN-MAT Holdings, LLC 23

Showing 12 of 780. All products under Cement, Dental

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K141503 2014-11-10
K132393 2014-03-14
K073101 2008-01-17

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