Data / Medical devices / Diluent, Blood Cell / United States

FDA-registered makers of Diluent, Blood Cell in the United States: 21 establishments

Name: FDA-registered makers of Diluent, Blood Cell in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in the United States are registered with the FDA to make Diluent, Blood Cell (product code GIF). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device: Diluent, Blood Cell
Product code: GIF
Country: United States

Makers of Diluent, Blood Cell in the United States

Maker	Location	Role	Recall events	Source
Abbott Laboratories	Irving, TX, United States	Specification developer	0	api.fda.gov
American Red Cross Diagnostic Manufacturing Divisi	Gaithersburg, MD, United States	Manufacturer	0	api.fda.gov
Azer Scientific, Inc.	Morgantown, PA, United States	Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer	0	api.fda.gov
Beckman Coulter, Inc.	Miami, FL, United States	Specification developer	2	api.fda.gov
Becton Dickinson	Franklin Lakes, NJ, United States	Specification developer	0	api.fda.gov
Beckman Coulter, Inc.	Hebron, KY, United States	Contract manufacturer	0	api.fda.gov
Clinical Diagnostic Solutions, Inc.	Plantation, FL, United States	Contract manufacturer, Manufacturer	0	api.fda.gov
Cliniqa Corporation	San Marcos, CA, United States	Manufacturer	0	api.fda.gov
E K Industries, Inc.	Joliet, IL, United States	Manufacturer	0	api.fda.gov
Fisher Diagnostics	Middletown, VA, United States	Contract manufacturer, Manufacturer	0	api.fda.gov
Hemo Bioscience	Durham, NC, United States	Complaint file establishment, Manufacturer	0	api.fda.gov
High Technology, Inc.	North Attleboro, MA, United States	Manufacturer	0	api.fda.gov
Immucor, Inc.	Norcross, GA, United States	Manufacturer	0	api.fda.gov
JAS Diagnostics/Drew Scientific	Plantation, FL, United States	Manufacturer	0	api.fda.gov
Medical Chemical Corporation	Torrance, CA, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Monobind, Inc.	Lake Forest, CA, United States	Manufacturer for export	0	api.fda.gov
Ortho-Clinical Diagnostics, Inc.	Rochester, NY, United States	Manufacturer	0	api.fda.gov
Ortho-Clinical Diagnostics, Inc.	Rochester, NY, United States	Specification developer	0	api.fda.gov
Sysmex Reagents America, Inc.	Mundelein, IL, United States	Contract manufacturer	0	api.fda.gov
Siemens Healthcare Diagnostics Inc.	Tarrytown, NY, United States	Complaint file establishment, Specification developer	0	api.fda.gov
Siemens Healthcare Diagnostics Inc.	E Walpole, MA, United States	Manufacturer, Repackager or relabeler, Specification developer	0	api.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.