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Data / Medical devices / Enzymatic, Carbon-Dioxide / United States

FDA-registered makers of Enzymatic, Carbon-Dioxide in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Enzymatic, Carbon-Dioxide (product code KHS). 11 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Enzymatic, Carbon-Dioxide
Product code
KHS
Country
United States

Makers of Enzymatic, Carbon-Dioxide in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer, Specification developer3May 10, 2010000api.fda.gov
Alfa WassermannWest Caldwell, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer2May 2, 2013000api.fda.gov
Cliniqa CorporationSan Marcos, CA, United StatesManufacturer2June 24, 1998000api.fda.gov
Horiba Instruments IncorporatedCanton, MI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler2April 30, 2007000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer2May 10, 2010000api.fda.gov
Abbott LaboratoriesIrving, TX, United StatesSpecification developer1May 4, 2006000api.fda.gov
Diazyme Laboratories, Inc.Poway, CA, United StatesManufacturer1July 21, 2006000api.fda.gov
Hemagen Diagnostics, Inc.Baltimore, MD, United StatesManufacturer1May 21, 2001000api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1December 3, 1992000api.fda.gov
Scientific Supplies & Technology, Inc.Doral, FL, United StatesRemanufacturer, Repackager or relabeler1December 15, 2010000api.fda.gov
Teco DiagnosticsAnaheim, CA, United StatesManufacturer1March 20, 1995000api.fda.gov
Abaxis, Inc.Union City, CA, United StatesManufacturer0000api.fda.gov
ELITechGroup IncLogan, UT, United StatesContract manufacturer0000api.fda.gov
Fisher DiagnosticsMiddletown, VA, United StatesManufacturer0000api.fda.gov
High Technology, Inc.North Attleboro, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Instrumentation Laboratory Co.Bedford, MA, United StatesManufacturer0000api.fda.gov
Instrumentation Laboratory Co.Orangeburg, NY, United StatesManufacturer0000api.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 StatesManufacturer0010api.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.