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Data / Medical devices / Blood Specimen Collection Convenience Kit (Excludes Hiv) / United States

FDA-registered makers of Blood Specimen Collection Convenience Kit (Excludes Hiv) in the United States: 29 establishments

29 establishments in the United States are registered with the FDA to make Blood Specimen Collection Convenience Kit (Excludes Hiv) (product code PQD). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Blood Specimen Collection Convenience Kit (Excludes Hiv)
Product code
PQD
Country
United States

Makers of Blood Specimen Collection Convenience Kit (Excludes Hiv) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aero-Med LLCEast Hartford, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
ALOM Technologies CorporationIndianapolis, IN, United StatesContract manufacturer0000api.fda.gov
Biodesix, Inc.Louisville, CO, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Disruptive Medtech, LLCLaramie, WY, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Enable BiosciencesSouth San Francisco, CA, United StatesSpecification developer0000api.fda.gov
Everly Health, Inc.Austin, TX, United StatesManufacturer0000api.fda.gov
Generation LabBurlingame, CA, United StatesManufacturer0000api.fda.gov
IMPILO, Inc.Philadelphia, PA, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
IxlayerSan Francisco, CA, United StatesSpecification developer0000api.fda.gov
Impilo PhoenixPhoenix, AZ, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Kit CompanyPhoenix, AZ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Kryocall LLC Dba KryosphereCary, NC, United StatesManufacturer0000api.fda.gov
Labcorp GeneticsSan Francisco, CA, United StatesSpecification developer0000api.fda.gov
MHC Health Management Solutions, LLCCape Coral, FL, United StatesSpecification developer0000api.fda.gov
NAR Medical Depot, LLCGreer, SC, United StatesManufacturer0000api.fda.gov
Neelyx LabsWood Dale, IL, United StatesManufacturer0000api.fda.gov
Precision For MedicineFrederick, MD, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Randox Laboratories-Us, LtdKearneysville, WV, United StatesManufacturer0000api.fda.gov
RenalytixaiLong Island City, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Roman Health Ventures Inc.New York, NY, United StatesSpecification developer0000api.fda.gov
Spectrum Solutions LLCDraper, UT, United StatesContract manufacturer0000api.fda.gov
Spot Health Inc.Cincinnati, OH, United StatesManufacturer0000api.fda.gov
Supera Fulfillment LLCHouston, TX, United StatesManufacturer0000api.fda.gov
Synchronis Medical LLCRomulus, MI, United StatesManufacturer0000api.fda.gov
Tasso IncSeattle, WA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
The Dot Printer Inc.Irvine, CA, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Vericel CorporationCambridge, MA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov

Updated November 3, 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.