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Data / Medical devices / Low Dead Space Needle, Single Lumen, Hypodermic

Low Dead Space Needle, Single Lumen, Hypodermic (QNS): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Low Dead Space Needle, Single Lumen, Hypodermic (product code QNS, 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 25, 2024, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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

Makers by country

CountryMakers
United States1
Japan1
China1

Makers of Low Dead Space Needle, Single Lumen, Hypodermic

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
Ocuject, LLCSan Diego, CA, United StatesSpecification developer1October 25, 2024000api.fda.gov
TSK Laboratory International Japan KKTochigi, JapanManufacturer1March 8, 2024000api.fda.gov
Zhejiang Kindly Medical Devices Co., LtdWENZHOU Zhejiang, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov

Updated October 25, 2024. 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.