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Data / Medical devices / Alkaline Picrate, Colorimetry, Creatinine

Alkaline Picrate, Colorimetry, Creatinine (CGX): 36 FDA-registered makers in 10 countries

36 establishments in 10 countries are registered with the FDA to make Alkaline Picrate, Colorimetry, Creatinine (product code CGX, Class 2, 21 CFR 862.1225). 24 of them have a 510(k) clearance or PMA approval on file and 4 have a recall event. The FDA has issued 159 510(k) clearances under this code, the latest on January 9, 2026, and lists 14 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
CGX
Device class
2
Regulation
862.1225
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
United States22
Ireland3
Germany2
United Kingdom2
Japan2
France1
Hungary1
Switzerland1
Canada1
Greece1

Makers of Alkaline Picrate, Colorimetry, Creatinine

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
Beckman Coulter, Inc.Brea, CA, United StatesManufacturer, Specification developer3June 1, 2007020api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer, Specification developer3December 4, 2024030api.fda.gov
Horiba Abx SASMONTPELLIER Herault, FranceManufacturer, Specification developer2April 30, 2012000api.fda.gov
Roche Diagnostics GMBHMANNHEIM Baden-Wurttemberg, GermanyExporter to the US, Manufacturer, Repackager or relabeler, Specification developer2September 8, 1995000api.fda.gov
SCITECK DiagnosticsFletcher, NC, United StatesManufacturer2March 6, 1997000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer2December 4, 2024010api.fda.gov
Abbott Ireland Diagnostics DivisionLongford, IrelandManufacturer1March 22, 2022000api.fda.gov
Abbott LaboratoriesIrving, TX, United StatesSpecification developer1April 7, 2009000api.fda.gov
Bialex LabWichita Falls, TX, United StatesManufacturer1May 15, 2013000api.fda.gov
Beckman Coulter Ireland IncO CALLAGHANS MILLS Clare, IrelandContract manufacturer, Manufacturer1October 19, 1992000api.fda.gov
Cliniqa CorporationSan Marcos, CA, United StatesManufacturer1April 18, 1984000api.fda.gov
Carolina Liquid ChemistriesBrea, CA, United StatesManufacturer1December 27, 2004000api.fda.gov
DIAMOND DIAGNOSTICS IncHolliston, MA, United StatesManufacturer1January 30, 2004000api.fda.gov
Diamond Diagnostics Inc.Budapest, HungaryContract manufacturer, Exporter to the US1September 8, 1995000api.fda.gov
Horiba Instruments IncorporatedCanton, MI, United StatesManufacturer1March 24, 1983020api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1February 24, 1998000api.fda.gov
Medica Corp.Bedford, MA, United StatesManufacturer1May 15, 2013000api.fda.gov
Nova Biomedical CorporationWaltham, MA, United StatesComplaint file establishment, Manufacturer1November 19, 2024000api.fda.gov
Randox Laboratories LimitedCRUMLIN, COUNTY ANTRIM Antrim and Newtownabbey, United KingdomContract manufacturer, Manufacturer1March 6, 1998000api.fda.gov
Roche Diagnostics GMBHPENZBERG Bavaria, GermanyManufacturer1September 8, 1995000api.fda.gov
Roche Diagnostics International Ltd.ROTKREUZ Zug, SwitzerlandManufacturer1September 8, 1995000api.fda.gov
Stanbio LaboratoryBoerne, TX, United StatesManufacturer1November 3, 1977000api.fda.gov
Sekisui Diagnostics P.E.I. Inc.CHARLOTTETOWN Prince Edward Island, CanadaContract manufacturer, Manufacturer1February 18, 2000000api.fda.gov
Teco DiagnosticsAnaheim, CA, United StatesManufacturer1March 23, 1988000api.fda.gov
Abaxis, Inc.Union City, CA, United StatesManufacturer0000api.fda.gov
Alfa WassermannWest Caldwell, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Beckman Coulter, Inc.Carlsbad, CA, United StatesContract manufacturer0000api.fda.gov
Beckman Coulter K. K.Sunto-Gun Shizuoka, JapanSpecification developer0000api.fda.gov
Beckman Coulter Mishima K.K.SUNTO-GUN Shizuoka, JapanContract manufacturer0000api.fda.gov
Depuy (ireland)CO. CORK Munster, IrelandManufacturer, Specification developer0000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesSpecification developer0000api.fda.gov
Fisher DiagnosticsMiddletown, VA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Medicon Hellas SAGERAKAS Attiki, GreeceManufacturer0000api.fda.gov
Nova Biomedical CorporationBillerica, MA, United StatesManufacturer for export0000api.fda.gov
Siemens Healthcare Diagnostics Manufacturing LtdSUDBURY Suffolk, United KingdomManufacturer0000api.fda.gov
Siemens Healthcare Diagnostics IncEast Walpole, MA, United StatesSpecification developer0000api.fda.gov

Updated January 9, 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.