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Data / Medical devices / China / Liaoning Upcera Co.,Ltd

Liaoning Upcera Co.,Ltd: FDA-registered device maker in Benxi Liaoning, China, 10 510(k) clearances

Liaoning Upcera Co.,Ltd is registered with the FDA (registration 3008254125) in Benxi Liaoning, China. It lists 10 device types. The FDA files 10 510(k) clearances under its listings, the newest dated March 2, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3008254125
Address
NO.122 Xianghuai Road Economic Development Zone, Benxi Liaoning, China, 117004
Owner or operator
Liaoning Upcera Co., Ltd (10031628)
Roles
Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer
First device listed
January 4, 2015
Registered through
2026
Brand names listed
Abrasive material Pulverized Corundum, Adhesive Tip Applicator, Binocular Loupe, Ceramic Etchant (HF-5 and HF-9), DUO,Aevra, Dental Lithium Disilicate Glass Ceramic Block (Up. Press Series and Up. CAD Series), FLNTScan R1;FLNTScan R1 Pro;FLNTScan R1 Cart;FLNTScan R2;FLNTScan R2 Pro;FLNTScan R2 Air;FLNTScan R2 Pod;FLNTScan R2 Car, Glaze Paste, Glaze Powder, and Glaze Liquid and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 2, 2026K253380“FLNT Base” and “FLNT Temp”EBGSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
January 9, 2026K253973Gradual Dental Zirconia Blank - GT(F) P1, GT(F) P2, and SP SeriesEIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
October 2, 2024K240153Ceramic Etchant (HF-5 and HF-9)KLESubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
September 7, 2023K231687Gradual Dental Zirconia BlankEIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
September 2, 2018K181167Upcera Glaze Paste, Glaze Powder, and Glaze LiquidEIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
January 12, 2017K162323Tooth Shade Resin MaterialEBFSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
December 4, 2015K152175Upcera Dental Zirconia Blank for Aesthetic RestorationEIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
December 18, 2014K141727DENTAL LITHIUM DISILICATE GLASS CERAMIC BLOCK (UP. PRESS SERIES AND UP. CAD SERIES)EIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
October 22, 2014K141724UPCERA DENTAL ZIRCONIA BLANK & DENTAL ZIRCONIA PRE-SHADED BLANKEIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov
October 22, 2014K141723UPCERA COLORING LIQUID (I AND II )EIHSubstantially EquivalentLiaoning Upcera Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.