GlasIonomer FX-LC

GlasIonomer FX-LC CAPSULE HV A2 3pcs (SAMPLE)

Registry build 21.09.26
3manufacturers in China registered for this device type
45catalogue numbers in this listing
24510(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 GlasIonomer FX-LC
Listed by Shofu Dental Corp., United States
FDA product code EMA
Device type Cement, Dental
Device class Class 2
Regulation 21 CFR 872.3275
Establishment Repacker / relabeller
510(k) K252808
Record published 2026-04-10

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, manufacturing date
Storage Storage environment temperature 1 to 25 °C

Catalogue Numbers

Catalogue numbers for GlasIonomer FX-LC
Catalogue number Size Per pack Status
C0086 In distribution
C0042 50 In distribution
C0060 50 In distribution
C0044 50 In distribution
C0061 50 In distribution
C0049 50 In distribution
C0075 In distribution
C0047 50 In distribution
C0043 50 In distribution
C0053 50 In distribution
C0045 50 In distribution
C0056 50 In distribution
C0076 In distribution
C0065 50 In distribution
C0066 50 In distribution
C0048 50 In distribution
C0054 50 In distribution
C0083 In distribution
C0059 50 In distribution
C0064 50 In distribution
C0073 In distribution
C0058 50 In distribution
C0055 50 In distribution
C0082 In distribution
C0084 In distribution
C0070 3 In distribution
C0080 In distribution
C0071 3 In distribution
C0081 In distribution
C0069 50 In distribution
C0079 In distribution
C0052 50 In distribution
C0057 50 In distribution
C0074 In distribution
C0063 50 In distribution
C0072 In distribution
C0085 In distribution
C0046 50 In distribution
C0062 50 In distribution
C0050 50 In distribution
C0051 50 In distribution
C0078 In distribution
C0068 50 In distribution
C0067 50 In distribution
C0077 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
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
TPH®3 flow Liquid Micro Hybrid Dentsply LLC 22

Showing 12 of 780. All products under Cement, Dental

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252808 2025-12-09
K252165 2025-10-28
K251470 2025-07-11
K233161 2023-09-28
K222253 2022-09-22
K120159 2012-06-18
K112307 2012-03-28
K111855 2011-11-17
K111685 2011-09-02
K080517 2008-06-11
K031467 2003-07-17
K002461 2000-09-26
K982461 1998-08-24
K971927 1997-06-30
K945451 1995-02-27
K940122 1994-05-02
K863141 1986-08-26
K862280 1986-06-23
K861005 1986-04-25
K850913 1985-04-10
K841195 1984-05-14
K841196 1984-05-11
K810765 1981-06-12
K810764 1981-06-12

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