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Data / Medical devices / Research Use Only/Hematology Devices

Research Use Only/Hematology Devices (OTQ): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Research Use Only/Hematology Devices (product code OTQ, Class N). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
OTQ
Device class
N
Medical specialty
Unknown

Makers by country

CountryMakers
United States2
Canada1
Hong Kong1

Makers of Research Use Only/Hematology Devices

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
Corgenix, Inc.Broomfield, CO, United StatesManufacturer for export0000api.fda.gov
Dna Genotek, Inc.Ottawa Ontario, CanadaManufacturer0000api.fda.gov
EmCyte CorporationFort Myers, FL, United StatesSpecification developer0000api.fda.gov
Phase Scientific International LimitedShatin NT, HONG KONG, Hong KongManufacturer0000api.fda.gov

Updated November 2, 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.