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Data / Medical devices / Photometric Method, Magnesium / United States

FDA-registered makers of Photometric Method, Magnesium in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Photometric Method, Magnesium (product code JGJ). 11 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Photometric Method, Magnesium
Product code
JGJ
Country
United States

Makers of Photometric Method, Magnesium in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott LaboratoriesIrving, TX, United StatesSpecification developer2September 12, 2018000api.fda.gov
Abaxis, Inc.Union City, CA, United StatesManufacturer1January 30, 2004000api.fda.gov
Alfa WassermannWest Caldwell, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer1August 27, 2012000api.fda.gov
Beckman Coulter, Inc.Brea, CA, United StatesManufacturer, Specification developer1January 27, 1989010api.fda.gov
Cliniqa CorporationSan Marcos, CA, United StatesManufacturer1January 21, 1988000api.fda.gov
Fisher DiagnosticsMiddletown, VA, United StatesContract manufacturer, Manufacturer1March 11, 1992000api.fda.gov
Horiba Instruments IncorporatedCanton, MI, United StatesManufacturer1September 16, 1985000api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1July 31, 1990000api.fda.gov
Stanbio LaboratoryBoerne, TX, United StatesManufacturer1February 7, 1989000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer1January 19, 2017000api.fda.gov
Teco DiagnosticsAnaheim, CA, United StatesManufacturer1December 18, 1987000api.fda.gov
Beckman Coulter, Inc.Carlsbad, CA, 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
Microgenics CorporationFremont, CA, United StatesContract manufacturer0000api.fda.gov
Ortho-Clinical Diagnostics, Inc.Rochester, NY, 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 StatesManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer, Specification developer0050api.fda.gov
Viant AS&O Holdings, LLCBrimfield, MA, United StatesContract manufacturer0000api.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.