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Data / Medical devices / Set, Tubing And Support, Ventilator (W Harness) / United States

FDA-registered makers of Set, Tubing And Support, Ventilator (W Harness) in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Set, Tubing And Support, Ventilator (W Harness) (product code BZO). 2 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.

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Get makers of this device in the United StatesWatch these makers
Device
Set, Tubing And Support, Ventilator (W Harness)
Product code
BZO
Country
United States

Makers of Set, Tubing And Support, Ventilator (W Harness) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1December 27, 1990010api.fda.gov
Thayer Medical CorportationTucson, AZ, United StatesManufacturer1July 18, 1988000api.fda.gov
ASP Global, LLCAustell, GA, United StatesSpecification developer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Bio-Med Devices, Inc.Guilford, CT, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
C2C Development, LLCMelbourne, FL, United StatesContract manufacturer0000api.fda.gov
Circuitlife LLCSan Antonio, TX, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
CovidienCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
CovidienLafayette, CO, United StatesSpecification developer0000api.fda.gov
DRW MedicalAston, PA, United StatesManufacturer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
Iilabco LLCBrea, CA, United StatesSpecification developer0000api.fda.gov
Instrumentation Industries, IncorporatedBethel Park, PA, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Intersurgical Inc.Indianapolis, IN, United StatesManufacturer0000api.fda.gov
King Systems Corporation.Noblesville, IN, United StatesManufacturer0000api.fda.gov
Mallinckrodt Manufacturing LLCMadison, WI, United StatesManufacturer0011api.fda.gov
Pepper Medical, Inc.West Chester, PA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Percussionaire Corp.Sandpoint, ID, United StatesManufacturer0022api.fda.gov
Respironics Inc.Murrysville, PA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Smooth-Bor PlasticsLaguna Hills, CA, United StatesManufacturer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesManufacturer0000api.fda.gov
Tri-Anim Health Services, Inc.Dublin, OH, United StatesSpecification developer0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Westmed, Inc.Tucson, AZ, United StatesContract manufacturer, Manufacturer0000api.fda.gov

Updated November 3, 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.