RelyX™

3M™ ESPE™ RelyX™ Try-In Paste A3 Opaque/Yellow Opaque Shade Syringe Refill, 7614A3T

Registry build 21.09.26
3manufacturers in China registered for this device type
14catalogue numbers in this listing
12510(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 RelyX™
Listed by 3M Company, United States
FDA product code EMA
Device type Cement, Dental
Device class Class 2
Regulation 21 CFR 872.3275
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-24
Record revised 2023-02-23 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 10

Catalogue Numbers

Catalogue numbers for RelyX™
Catalogue number Size Per pack Status
3505L In distribution
3525TK In distribution
7614A1T In distribution
3535TK In distribution
7614WOT In distribution
7614B0.5T In distribution
7614A3T In distribution
3505 In distribution
3535 In distribution
3535SK In distribution
7614A5T In distribution
7614TRT In distribution
3505P In distribution
3525 2 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
K170330 2017-02-06
K052235 2005-09-27
K022476 2002-08-02
K011200 2001-06-14
K002452 2000-09-28
K973961 1997-12-17
K962065 1996-07-18
K933139 1994-01-05
K925032 1992-12-23
K911842 1991-06-17
K902041 1990-06-27
K864270 1986-12-16

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