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Data / Medical devices / Bronchoscope (Flexible Or Rigid) / United States

FDA-registered makers of Bronchoscope (Flexible Or Rigid) in the United States: 33 establishments

33 establishments in the United States are registered with the FDA to make Bronchoscope (Flexible Or Rigid) (product code EOQ). 23 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Bronchoscope (Flexible Or Rigid)
Product code
EOQ
Country
United States

Makers of Bronchoscope (Flexible Or Rigid) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Karl Storz Endoscopy-America, Inc.Auburn, MA, United StatesContract manufacturer, Repackager or relabeler13December 5, 2025000api.fda.gov
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesSpecification developer11September 23, 2025050api.fda.gov
Boston Scientific CorporationMarlborough, MA, United StatesComplaint file establishment, Specification developer6March 2, 2023000api.fda.gov
Auris Health, IncSanta Clara, CA, United StatesManufacturer, Specification developer5July 25, 2026040api.fda.gov
Auris Health, Inc.San Jose, CA, United StatesManufacturer, Repackager or relabeler5July 25, 2026000api.fda.gov
Broncus Medical IncSan Jose, CA, United StatesManufacturer5May 31, 2024000api.fda.gov
Intuitive Surgical, Inc.Santa Clara, CA, United StatesManufacturer4September 23, 2025000api.fda.gov
Covidien llcPlymouth, MN, United StatesManufacturer, Specification developer3April 21, 2017000api.fda.gov
Boston Scientific CorporationCoventry, RI, United StatesManufacturer2March 8, 2019000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer2November 22, 1994010api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer2November 22, 1994000api.fda.gov
Boston Scientific CorporationSpencer, IN, United StatesManufacturer1March 27, 2017000api.fda.gov
Contra Healthcare Solutions LLCButler, PA, United StatesManufacturer, Specification developer1April 30, 2025000api.fda.gov
Mercator Medsystems, Inc.San Leandro, CA, United StatesManufacturer1July 2, 2013000api.fda.gov
NOAH MEDICAL Corp.San Jose, CA, United StatesManufacturer1March 1, 2023050api.fda.gov
NOAH MEDICAL Corp.San Carlos, CA, United StatesSpecification developer1March 1, 2023000api.fda.gov
NOAH MEDICAL Corp.Sunnyvale, CA, United StatesComplaint file establishment, Specification developer1March 1, 2023000api.fda.gov
OTU Medical IncUnion City, CA, United StatesManufacturer, Specification developer1June 16, 2022000api.fda.gov
Serpex Medical, Inc.Santa Clara, CA, United StatesComplaint file establishment, Specification developer1August 15, 2022000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesSpecification developer1May 22, 2009000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler1July 19, 1976000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1July 19, 1976000api.fda.gov
Wilson-Cook Medical Inc.Winston Salem, NC, United StatesComplaint file establishment, Manufacturer1February 21, 2018000api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer for export0000api.fda.gov
Centerpoint Systems LLCWest Valley City, UT, United StatesContract manufacturer0000api.fda.gov
Cogentix Medical, Inc.Orangeburg, NY, United StatesSpecification developer0000api.fda.gov
Command Medical Products, LLC.Ormond Beach, FL, United StatesContract manufacturer0000api.fda.gov
Creation TechnologiesEverett, WA, United StatesContract manufacturer0000api.fda.gov
Harwood Design, Inc.Bristol, PA, United StatesContract manufacturer0000api.fda.gov
Hobbs Medical, Inc.Stafford Springs, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Karl Storz Endovision, Inc.Charlton, MA, United StatesContract manufacturer0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Viant AS&O Holdings, LLCLaconia, NH, United StatesContract manufacturer0000api.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.