Data / Medical devices / Ph Buffer / United States

FDA-registered makers of Ph Buffer in the United States: 27 establishments

Name: FDA-registered makers of Ph Buffer in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

27 establishments in the United States are registered with the FDA to make Ph Buffer (product code JCC). 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: Ph Buffer
Product code: JCC
Country: United States

Makers of Ph Buffer in the United States

Maker	Location	Role	Recall events	Source
Abbott Laboratories	Irving, TX, United States	Specification developer	0	api.fda.gov
Biocare Medical, LLC	Pacheco, CA, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Biogenex Laboratories Inc.	Fremont, CA, United States	Manufacturer	0	api.fda.gov
Bion Enterprises, Ltd.	Des Plaines, IL, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Biovire, Inc.	Brighton, MI, United States	Contract manufacturer	0	api.fda.gov
Chemical Service Labs, LLC	Dallas, TX, United States	Manufacturer	0	api.fda.gov
CalibreScientific US, Inc.	Vancouver, WA, United States	Manufacturer	0	api.fda.gov
Diagnostic Biosystems	Pleasanton, CA, United States	Manufacturer	0	api.fda.gov
Empire Genomics Corp.	Depew, NY, United States	Manufacturer	0	api.fda.gov
ENG Scientific LLC	New Brunswick, NJ, United States	Manufacturer	0	api.fda.gov
Ethos Biosciences, INC.	Logan Township, NJ, United States	Contract manufacturer, Manufacturer	0	api.fda.gov
Fisher Diagnostics	Middletown, VA, United States	Manufacturer	0	api.fda.gov
Immucor, Inc.	Norcross, GA, United States	Manufacturer	0	api.fda.gov
Medical Chemical Corporation	Torrance, CA, United States	Manufacturer	0	api.fda.gov
Mesa Laboratories, Inc.	Denver, CO, United States	Manufacturer	1	api.fda.gov
Newcomer Supply Inc	Waunakee, WI, United States	Specification developer	0	api.fda.gov
Premier Dental Products Co.	Plymouth Meeting, PA, United States	Complaint file establishment, Specification developer	0	api.fda.gov
Premier Medical	Philadelphia, PA, United States	Contract manufacturer	0	api.fda.gov
Reprocessing Products Corporation (RPC)	Tucson, AZ, United States	Complaint file establishment, Manufacturer	0	api.fda.gov
Richard-Allan Scientific LLC	Kalamazoo, MI, United States	Contract manufacturer, Manufacturer	0	api.fda.gov
Rocky Mountain Reagents, Inc.	Golden, CO, United States	Complaint file establishment, Contract manufacturer, Manufacturer	0	api.fda.gov
Scytek Laboratories, Inc.	Logan, UT, United States	Manufacturer	0	api.fda.gov
Sigma-Aldrich Manufacturing, LLC	St. Louis, MO, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov
Sigma-Aldrich Manufacturing, LLC-H&H	Saint Louis, MO, United States	Manufacturer	0	api.fda.gov
Ventana Medical Systems, Inc.	Tucson, AZ, United States	Manufacturer	0	api.fda.gov
Volusol	Tooele, UT, United States	Manufacturer	0	api.fda.gov
Zeta Corporation	Monrovia, CA, United States	Manufacturer, Remanufacturer	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.