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Data / Medical devices / Ophthalmic Needle

Ophthalmic Needle (QYM): 4 FDA-registered makers in 4 countries

4 establishments in 4 countries are registered with the FDA to make Ophthalmic Needle (product code QYM, Class 2, 21 CFR 880.5570). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on October 6, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
QYM
Device class
2
Regulation
880.5570
Medical specialty
General Hospital

Makers by country

CountryMakers
Belgium1
Japan1
United States1
China1

Makers of Ophthalmic Needle

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Terumo Europe N.V.LEUVEN Vlaams Brabant, BelgiumManufacturer1October 18, 2023000api.fda.gov
TSK Laboratory International Japan KKTochigi, JapanManufacturer1October 23, 2024000api.fda.gov
Ocuject, LLCSan Diego, CA, United StatesSpecification developer0000api.fda.gov
Zhejiang Kindly Medical Devices Co., LtdWENZHOU Zhejiang, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov

Updated October 6, 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.