Correct Plus

Mighty Mix; Hydrophilic Vinyl Polysiloxane Impression Material; 5:1 Cartridge System; Universal Body

Registry build 21.09.26
6manufacturers in China registered for this device type
29catalogue numbers in this listing
8510(k) clearances naming this product code
2recalls 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 Correct Plus
Listed by Kerr Corporation, United States
FDA product code ELW
Device type Material, Impression
Device class Class 2
Regulation 21 CFR 872.3660
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-08-01
Record revised 2021-12-10 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Store at ambient temperature
Sizes Total volume 200 to 1600 ml

Catalogue Numbers

Catalogue numbers for Correct Plus
Catalogue number Size Per pack Status
Q34JC Total Volume 1600 ml 32 In distribution
Q34JA Total Volume 200 ml 4 In distribution
Q34H Total Volume 460 ml In distribution
Q34HC Total Volume 1600 ml 32 In distribution
Q34HAA Total Volume 200 ml 4 In distribution
Q36CC Total Volume 1600 ml 32 In distribution
Q34JAA Total Volume 200 ml 4 In distribution
Q34MC Total Volume 760 ml 2 In distribution
Q34DC Total Volume 1600 ml 32 In distribution
Q34MA Total Volume 760 ml 2 In distribution
Q36A Total Volume 200 ml 4 In distribution
Q36B Total Volume 200 ml 4 In distribution
Q34HAC Total Volume 1600 ml 32 In distribution
Q34JAC Total Volume 1600 ml 32 In distribution
Q36BB Total Volume 1600 ml 32 In distribution
Q34HCA Total Volume 460 ml In distribution
Q36C Total Volume 200 ml 4 In distribution
Q34MB Total Volume 760 ml 2 In distribution
Q36MB Total Volume 760 ml 2 In distribution
Q34BC Total Volume 1600 ml 32 In distribution
Q34IA Total Volume 200 ml 4 In distribution
Q34IC Total Volume 1600 ml 32 In distribution
Q34HA Total Volume 200 ml 4 In distribution
Q34GC Total Volume 1600 ml 32 In distribution
Q36AA Total Volume 1600 ml 32 In distribution
Q34BA Total Volume 200 ml 4 In distribution
Q34GA Total Volume 200 ml 4 In distribution
Q34DA Total Volume 200 ml 4 In distribution
Q36MA Total Volume 760 ml 2 In distribution

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
K160441 2016-06-30
K110092 2011-04-08
K092176 2010-01-28
K091613 2009-10-07
K072622 2007-12-04
K031484 2003-07-03
K010994 2001-04-23
K001655 2000-08-10

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
2012-02-21 Class II Nonconforming Material/Component The firm recalled the product because it may cure harder than expected within the
shelf life, which could result in a material that may be more difficult to remove. Use of this product on
patients with loose teeth may result in possible too
45 kits and 87 refills 2012-11-15
2010-11-04 Not classified Packaging process control Pentron Clinical is voluntarily recalling the following lot of mislabeled Correct VPS Medium Body Tubes. It was discovered that the individual tubes inside the Correct VPS Medium Body Tube boxes are missing the lot/expiration date sticker. 176 units 2012-03-14

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