Geristore®

Geristor SY SMP A2 BAG 1FLW IT

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 Geristore®
Listed by DEN-MAT Holdings, LLC, United States
FDA product code EMA
Device type Cement, Dental
Device class Class 2
Regulation 21 CFR 872.3275
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-24
Record revised 2023-09-11 (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
Storage Special storage condition: Do not freeze; Special storage condition: Do not expose to direct sunlight; Storage environment temperature 47 to 77 °F; Handling environment temperature 47 to 77 °F

Catalogue Numbers

Catalogue numbers for Geristore®
Catalogue number Size Status
030451110 In distribution
034524101 In distribution
034523101 In distribution
039845730 In distribution
031479300 In distribution
031457730 In distribution
034526101B In distribution
031457520 In distribution
030450911B In distribution
031477100 In distribution
031458550 In distribution
031476110 In distribution
034522101 In distribution
031457500 In distribution
031457720 In distribution
4506 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
K881918 1988-07-15
K852196 1985-06-20

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