Data / Medical devices / Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature (FMK): 65 FDA-registered makers in 16 countries

65 establishments in 16 countries are registered with the FDA to make Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature (product code FMK, Class 2, 21 CFR 878.4850). 36 of them have a 510(k) clearance or PMA approval on file and 3 have a recall event. The FDA has issued 111 510(k) clearances under this code, the latest on September 13, 2026, and lists 12 recall events (0 Class I). FDA data exported November 3, 2026.

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Product code

FMK

Device class

2

Regulation

878.4850

Medical specialty

General, Plastic Surgery

Makers by country

Makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

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.

Updated September 13, 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.