Data / Medical devices / Support, Breathing Tube / United States

FDA-registered makers of Support, Breathing Tube in the United States: 19 establishments

Name: FDA-registered makers of Support, Breathing Tube in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in the United States are registered with the FDA to make Support, Breathing Tube (product code JAY). 1 has 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: Support, Breathing Tube
Product code: JAY
Country: United States

Makers of Support, Breathing Tube in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
B & B Medical Technologies, Inc.	Carlsbad, CA, United States	Specification developer	1	October 20, 1987	0	api.fda.gov
Acanthus Medical Creations, LLC	Wauconda, IL, United States	Manufacturer, Specification developer	0		0	api.fda.gov
Anesthesia Associates, Inc.	San Marcos, CA, United States	Contract manufacturer, Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Bird & Cronin, LLC	Eagan, MN, United States	Manufacturer	0		0	api.fda.gov
DRW Medical	Aston, PA, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Global Respiratory Solutions, Inc. (dba) Respiralogics	Reno, NV, United States	Specification developer	0		0	api.fda.gov
Icu Medical, Inc.	San Clemente, CA, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Inhalation Plastics, Inc.	Pittsburgh, PA, United States	Manufacturer	0		0	api.fda.gov
Instrumentation Industries, Incorporated	Bethel Park, PA, United States	Manufacturer	0		1	api.fda.gov
Larynnovation, Inc	La Jolla, CA, United States	Manufacturer	0		0	api.fda.gov
Marketlab Incorporated	Caledonia, MI, United States	Manufacturer	0		0	api.fda.gov
Marpac, Inc.	Albuquerque, NM, United States	Manufacturer	0		0	api.fda.gov
Neotech Products, LLC	Valencia, CA, United States	Manufacturer, Repackager or relabeler, Specification developer	0		0	api.fda.gov
Pepper Medical, Inc.	West Chester, PA, United States	Repackager or relabeler, Specification developer	0		0	api.fda.gov
Pryor Products	Oceanside, CA, United States	Contract manufacturer	0		0	api.fda.gov
Tarry Medical Products, Inc.	Danbury, CT, United States	Contract manufacturer	0		0	api.fda.gov
Teleflex Medical LLC	Morrisville, NC, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
W.T. Farley, Inc.	Ladson, SC, United States	Specification developer	0		0	api.fda.gov
Westmed, Inc.	Tucson, AZ, United States	Manufacturer	0		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.