Virtual XD

Virtual XD 380 Refill Heavy Body R 2X380

Registry build 21.09.26
6manufacturers in China registered for this device type
35catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Henan (1), Shandong (1), Jiangxi (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code ELW
Manufacturer City Province Registered as Device types
Hygedent Inc. Beijing Beijing Contract manufacturer 1
Zhengzhou Huaer Electro-Optics Technology Co., Ltd. Zhengzhou Henan Contract manufacturer 21
Shandong Huge Dental Material Corporation Rizhao Shandong Manufacturer 17
Jiangxi Dentalbright Technology Co., Ltd. Jiujiang Jiangxi Contract manufacturer 12
Sunrise Dental Laboratory, Ltd. Kowloon Hong Kong Manufacturer 5
Chemoment Materials Co., Ltd. Hefei Anhui Manufacturer 3

Record

Regulatory record for Virtual XD
Listed by Ivoclar Vivadent, Inc., Canada
FDA product code ELW
Device type Material, Impression
Device class Class 2
Regulation 21 CFR 872.3660
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-04-07
Record revised 2023-11-21 (version 5)

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
Distribution end date 2023-11-20

Catalogue Numbers

Catalogue numbers for Virtual XD
Catalogue number Size Status
646468 In distribution
646469 In distribution
646462 In distribution
646449 In distribution
646448 In distribution
646465 In distribution
646467 In distribution
646460 In distribution
646459 In distribution
646466 In distribution
646461 In distribution
646455 Withdrawn
646459 Withdrawn
646456 Withdrawn
646457 Withdrawn
646454 Withdrawn
646463 Withdrawn
646449 Withdrawn
646465 Withdrawn
646437 Withdrawn
646435 Withdrawn
646451 Withdrawn
646436 Withdrawn
646466 Withdrawn
646452 Withdrawn
646458 Withdrawn
646467 Withdrawn
646464 Withdrawn
646468 Withdrawn
646453 Withdrawn
646461 Withdrawn
646462 Withdrawn
646448 Withdrawn
646460 Withdrawn
646450 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Henry Schein Henry Schein, Inc. 164
Darby Dental Supply, LLC Darby Dental Supply, LLC 124
EXAlence™ GC America Inc. 96
MARK3 Cargus International, Inc 75
Panasil Kettenbach Gmbh & Co KG 73
Aquasil Ultra Smart Wetting® Impression Material Cartridge System Dentsply LLC 72
DentMix IPB Inc 70
Affinis Coltène/Whaledent AG 67
Take 1 Advanced Kerr Corporation 54
MDC Dental MDC Dental 49
Elastomeric Impression Material Shandong Huge Dental Material Corporation 46
Splash® DEN-MAT Holdings, LLC 44

Showing 12 of 1,245. All products under Material, Impression

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K143575 2015-04-03
K060891 2006-07-17

Recalls

3 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
2016-11-09 Class II Under Investigation by firm The firm received complaints claiming the dental material failed to set up. As the dental material ages, the set time may increase. US: 2090 units, Canada: 331 units, Australia: 465 units 2018-06-18
2016-11-09 Class II Under Investigation by firm The firm received complaints claiming the dental material failed to set up. As the dental material ages, the set time may increase. US: 4659 units, Canada: 729 units 2018-06-18
2016-11-09 Class II Under Investigation by firm The firm received complaints claiming the dental material failed to set up. As the dental material ages, the set time may increase. US: 1867 units, Canada: 465 units 2018-06-18

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