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Data / Medical devices / Phosphomolybdate (Colorimetric), Inorganic Phosphorus / United States

FDA-registered makers of Phosphomolybdate (Colorimetric), Inorganic Phosphorus in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Phosphomolybdate (Colorimetric), Inorganic Phosphorus (product code CEO). 10 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
Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Product code
CEO
Country
United States

Makers of Phosphomolybdate (Colorimetric), Inorganic Phosphorus in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Teco DiagnosticsAnaheim, CA, United StatesManufacturer2January 22, 1992000api.fda.gov
Abaxis, Inc.Union City, CA, United StatesManufacturer1September 5, 2002000api.fda.gov
Abbott LaboratoriesIrving, TX, United StatesSpecification developer1June 16, 1998000api.fda.gov
Beckman Coulter, Inc.Brea, CA, United StatesManufacturer, Specification developer1August 18, 2004010api.fda.gov
Cliniqa CorporationSan Marcos, CA, United StatesManufacturer1January 3, 1985000api.fda.gov
Hemagen Diagnostics, Inc.Baltimore, MD, United StatesManufacturer1October 25, 2000000api.fda.gov
Horiba Instruments IncorporatedCanton, MI, United StatesManufacturer1September 14, 1982000api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1July 17, 1991000api.fda.gov
Ortho-Clinical Diagnostics, Inc.Rochester, NY, United StatesSpecification developer1August 3, 1993010api.fda.gov
Ortho-Clinical Diagnostics, Inc.Rochester, NY, United StatesManufacturer1August 3, 1993000api.fda.gov
Alfa WassermannWest Caldwell, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0010api.fda.gov
Beckman Coulter, Inc.Carlsbad, CA, United StatesContract manufacturer0000api.fda.gov
Bialex LabWichita Falls, TX, United StatesManufacturer0000api.fda.gov
Fisher DiagnosticsMiddletown, VA, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
High Technology, Inc.North Attleboro, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Medica Corp.Bedford, MA, United StatesManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer, Specification developer0010api.fda.gov
Stanbio LaboratoryBoerne, TX, United StatesManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.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.