Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by U.S. FDA.
Listings on file with FDA
Device Name
Product Code
Status
Last Validated
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
FMK
Valid
April 24, 2024
Device Listing
Device Name
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Product Code
FMK
Company Function(s)
Repackager/Relabeler
Proprietary Name(s)
YORKTEST
LORISIAN
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