Data / Medical devices / Condenser, Heat And Moisture (Artificial Nose) / United States

FDA-registered makers of Condenser, Heat And Moisture (Artificial Nose) in the United States: 18 establishments

Name: FDA-registered makers of Condenser, Heat And Moisture (Artificial Nose) in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in the United States are registered with the FDA to make Condenser, Heat And Moisture (Artificial Nose) (product code BYD). 3 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: Condenser, Heat And Moisture (Artificial Nose)
Product code: BYD
Country: United States

Makers of Condenser, Heat And Moisture (Artificial Nose) in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Class I	Source
Covidien	Lafayette, CO, United States	Specification developer	4	June 8, 1995	0	0	api.fda.gov
Teleflex Medical LLC	Morrisville, NC, United States	Complaint file establishment, Specification developer	2	June 12, 1995	4	1	api.fda.gov
Icu Medical, Inc.	San Clemente, CA, United States	Complaint file establishment, Specification developer	1	January 19, 1988	0	0	api.fda.gov
ASP Global, LLC	Austell, GA, United States	Specification developer	0		0	0	api.fda.gov
Bruce Medical Supply	Waltham, MA, United States	Manufacturer	0		0	0	api.fda.gov
Dujo Logos Inc. DBA: MEDICOMP MEDICAL	Princeton, MN, United States	Contract manufacturer, Manufacturer	0		0	0	api.fda.gov
Freudenberg Medical, LLC	Carpinteria, CA, United States	Contract manufacturer, Manufacturer	0		0	0	api.fda.gov
Freudenberg Medical, LLC	Baldwin Park, CA, United States	Contract manufacturer	0		0	0	api.fda.gov
Intechrity Inc	Irvine, CA, United States	Contract manufacturer	0		0	0	api.fda.gov
Intersurgical Inc.	Indianapolis, IN, United States	Specification developer	0		0	0	api.fda.gov
King Systems Corporation.	Noblesville, IN, United States	Manufacturer, Repackager or relabeler, Specification developer	0		0	0	api.fda.gov
Passy-Muir, Inc.	Irvine, CA, United States	Manufacturer, Specification developer	0		0	0	api.fda.gov
Pepper Medical, Inc.	West Chester, PA, United States	Repackager or relabeler, Specification developer	0		0	0	api.fda.gov
Shikani Medical LLC	Lutherville, MD, United States	Specification developer	0		0	0	api.fda.gov
Somnetics International, Inc	Fridley, MN, United States	Specification developer	0		0	0	api.fda.gov
SunMed Group Holdings, LLC	Grand Rapids, MI, United States	Complaint file establishment, Specification developer	0		0	0	api.fda.gov
Thermedia Corporation	Shelton, WA, United States	Contract manufacturer, Manufacturer	0		0	0	api.fda.gov
Westmed, Inc.	Tucson, AZ, United States	Contract manufacturer, Manufacturer	0		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.