Riva Luting

Riva Luting Plus PWD REF 25G

Registry build 21.09.26
3manufacturers in China registered for this device type
16catalogue numbers in this listing
2510(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 Riva Luting
Listed by SDI Ltd., Australia
FDA product code EMA
Device type Cement, Dental
Device class Class 2
Regulation 21 CFR 872.3275
Establishment Manufacturer
510(k) K040393
Record published 2016-10-07
Record revised 2025-01-10 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Handling environment atmospheric pressure 5 to 25 °C
Distribution end date 2025-01-09

Catalogue Numbers

Catalogue numbers for Riva Luting
Catalogue number Size Per pack Status
8650508 In distribution
8651008 In distribution
8650008 In distribution
8651108 In distribution
8650108 In distribution
RIVA LUTING PLUS LQD REF 10G In distribution
RIVA LUTING LQD REF 25G In distribution
8651508 In distribution
8650510 In distribution
RIVA LUTING LY 50 CAP 50 Withdrawn
RIVA LUTING LY PWD REF 35 Withdrawn
RIVA LUTING PLUS P/L KT Withdrawn
RIVA LUTING P/L TRIPLE PK 3 Withdrawn
RIVA LUTING P/L KT LARGE Withdrawn
RIVA LUTING PLUS PWD REF 25G Withdrawn
RIVA LUTING PLUS 50 CAP 50 Withdrawn

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
K214118 2022-08-30
K073043 2007-12-14

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