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Data / Medical devices / Nadh Oxidation/Nad Reduction, Ast/Sgot / United States

FDA-registered makers of Nadh Oxidation/Nad Reduction, Ast/Sgot in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Nadh Oxidation/Nad Reduction, Ast/Sgot (product code CIT). 8 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Nadh Oxidation/Nad Reduction, Ast/Sgot
Product code
CIT
Country
United States

Makers of Nadh Oxidation/Nad Reduction, Ast/Sgot in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott LaboratoriesIrving, TX, United StatesSpecification developer2March 19, 2008000api.fda.gov
Horiba Instruments IncorporatedCanton, MI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler2December 21, 2001020api.fda.gov
Teco DiagnosticsAnaheim, CA, United StatesManufacturer2June 29, 1998000api.fda.gov
Bialex LabWichita Falls, TX, United StatesManufacturer1December 22, 1981000api.fda.gov
Cliniqa CorporationSan Marcos, CA, United StatesManufacturer1February 18, 1982000api.fda.gov
Carolina Liquid ChemistriesBrea, CA, United StatesManufacturer1January 17, 1997000api.fda.gov
Fisher DiagnosticsMiddletown, VA, United StatesContract manufacturer, Manufacturer, Manufacturer for export1May 23, 1996000api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1January 27, 1992000api.fda.gov
Abaxis, Inc.Union City, CA, United StatesManufacturer0000api.fda.gov
Alfa WassermannWest Caldwell, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0010api.fda.gov
Beckman Coulter, Inc.Brea, CA, United StatesSpecification developer0000api.fda.gov
Beckman Coulter, Inc.Carlsbad, CA, United StatesContract manufacturer0000api.fda.gov
ELITechGroup IncLogan, UT, United StatesContract manufacturer0000api.fda.gov
High Technology, Inc.North Attleboro, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Medica Corp.Bedford, MA, United StatesManufacturer0000api.fda.gov
Ortho-Clinical Diagnostics, Inc.Rochester, NY, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Ortho-Clinical Diagnostics, Inc.Rochester, NY, United StatesManufacturer, Manufacturer for export0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer, Specification developer0000api.fda.gov
Stanbio LaboratoryBoerne, TX, United StatesManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0010api.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.