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Data / Medical devices / Stylet, Tracheal Tube / United States

FDA-registered makers of Stylet, Tracheal Tube in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Stylet, Tracheal Tube (product code BSR). 5 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Stylet, Tracheal Tube
Product code
BSR
Country
United States

Makers of Stylet, Tracheal Tube in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer1August 11, 2017000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer1August 11, 2017000api.fda.gov
Cook IncorporatedCanton, IL, United StatesManufacturer1August 11, 2017000api.fda.gov
Medtronic Xomed, Inc.Jacksonville, FL, United StatesManufacturer1October 4, 1984000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler1August 8, 1995000api.fda.gov
Anamed, LLCCharlotte, NC, United StatesSpecification developer0000api.fda.gov
Anesthesia Associates, Inc.San Marcos, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
CovidienLafayette, CO, United StatesSpecification developer0010api.fda.gov
D R Burton Healthcare, LLCFarmville, NC, United StatesSpecification developer0000api.fda.gov
Gardner Medical Instruments, LLCFrankfort, IL, United StatesSpecification developer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
MedSource Labs, LLCChanhassen, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
NeVap Inc Inventory ManagementSan Jose, CA, United StatesSpecification developer0000api.fda.gov
One-AI Healthcare, IncRedmond, WA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
Robling Medical, LLCYoungsville, NC, United StatesContract manufacturer0000api.fda.gov
Sterramed IncWeehawken, NJ, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Salter LabsEl Paso, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Contract manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Through The Cords, LLCWest Jordan, UT, United StatesSpecification developer0000api.fda.gov
Truer Medical, Inc.Orange, CA, United StatesManufacturer0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0030api.fda.gov
WM&DGNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
Xponent Healthcare IncHudson, MA, United StatesManufacturer0000api.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.