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Data / Medical devices / China / Champion Optical Co., Ltd.

Champion Optical Co., Ltd.: FDA-registered device maker in DANYANG Jiangsu, China, 1 510(k) clearance

Champion Optical Co., Ltd. is registered with the FDA (registration 2000017897) in DANYANG Jiangsu, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 19, 1988. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2000017897
Address
No.88 Dangui Road Development Zone, DANYANG Jiangsu, China, 212300
Owner or operator
CHAMPION OPTICAL CO., LTD. (9087988)
Roles
Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler
First device listed
June 1, 2006
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Clip, Lens, Trial, OphthalmicHPB1Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Lens, Spectacle, Non-Custom (Prescription)HQG1Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov

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
April 19, 1988K881225OPHTHALMIC SPECTACLE LENS BLANKSHQGSubstantially EquivalentBeta Optical Co, Inc.accessdata.fda.gov

Compare with other makers

Updated April 19, 1988. 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.