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Data / Medical devices / Catheters, Suction, Tracheobronchial / United States

FDA-registered makers of Catheters, Suction, Tracheobronchial in the United States: 35 establishments

35 establishments in the United States are registered with the FDA to make Catheters, Suction, Tracheobronchial (product code BSY). 6 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 3, 2026.

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Device
Catheters, Suction, Tracheobronchial
Product code
BSY
Country
United States

Makers of Catheters, Suction, Tracheobronchial in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CovidienLafayette, CO, United StatesSpecification developer1November 25, 2003000api.fda.gov
Em Innovations, Inc.Galloway, OH, United StatesSpecification developer1July 14, 1988000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer1July 12, 1990000api.fda.gov
Neotech Products, LLCValencia, CA, United StatesManufacturer, Repackager or relabeler, Specification developer1June 19, 1986000api.fda.gov
Nurse Assist, LLCHaltom City, TX, United StatesManufacturer1February 12, 1985000api.fda.gov
Utah Medical Products, Inc.Midvale, UT, United StatesManufacturer1June 1, 1989000api.fda.gov
Amarigo IncLos Angeles, CA, United StatesManufacturer0000api.fda.gov
Ashtel Studios, Inc.Ontario, CA, United StatesSpecification developer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesSpecification developer0000api.fda.gov
Avanos Medical, Inc.Alpharetta, GA, United StatesSpecification developer0092api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesContract sterilizer, Specification developer0010api.fda.gov
Centurion Medical Products, LPHowell, MI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
CHS USA IncorporatedPeachtree City, GA, United StatesSpecification developer0000api.fda.gov
CMC Manufacturing LLC Dba CMC Med SolutionsSanford, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Dechoker LLCWheat Ridge, CO, United StatesManufacturer0000api.fda.gov
FridaBaby LLCMiami, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0061api.fda.gov
NDH Medical, Inc.Saint Petersburg, FL, United StatesContract manufacturer0000api.fda.gov
NJR Medical, Inc.Boynton Beach, FL, United StatesManufacturer0000api.fda.gov
North American Rescue, LLC.Greer, SC, United StatesSpecification developer0000api.fda.gov
NeVap Inc Inventory ManagementSan Jose, CA, United StatesSpecification developer0000api.fda.gov
Ouachita Contract Manufacturing, LLCMonroe, LA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Pepper Medical, Inc.West Chester, PA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Plastics Plus Technology, Inc.Redlands, CA, United StatesContract manufacturer0000api.fda.gov
Quick Aid LLCClearwater, FL, United StatesSpecification developer0000api.fda.gov
Sam Medical ProductsTualatin, OR, United StatesContract manufacturer0000api.fda.gov
Spiracle TechnologyLos Alamitos, CA, United StatesSpecification developer0000api.fda.gov
Splash Medical Devices, LLCAtlanta, GA, United StatesSpecification developer0000api.fda.gov
Sscor, Inc.Simi Valley, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
TMF Plastic Solutions LLCBradenton, FL, United StatesContract manufacturer0000api.fda.gov
Trinity Sterile, Inc.Salisbury, MD, United StatesManufacturer0000api.fda.gov
Vygon MFGDover, NH, United StatesManufacturer0000api.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.