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Data / Medical devices / Endoscope Channel Accessory / United States

FDA-registered makers of Endoscope Channel Accessory in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Endoscope Channel Accessory (product code ODC). 13 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
Endoscope Channel Accessory
Product code
ODC
Country
United States

Makers of Endoscope Channel Accessory in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
United States Endoscopy Group, Inc.Mentor, OH, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer10October 11, 2024000api.fda.gov
Medivators IncConroe, TX, United StatesManufacturer, Specification developer9November 8, 2024000api.fda.gov
Boston Scientific CorporationMarlborough, MA, United StatesComplaint file establishment, Specification developer5October 9, 2025010api.fda.gov
Boston Scientific CorporationCoventry, RI, United StatesManufacturer5October 9, 2025000api.fda.gov
Boston Scientific CorporationJohns Creek, GA, United StatesManufacturer2October 9, 2025000api.fda.gov
Boston Scientific CorporationSpencer, IN, United StatesManufacturer2March 27, 2001000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer2July 26, 2018000api.fda.gov
The Ruhof CorporationMineola, NY, United StatesComplaint file establishment, Manufacturer2October 16, 2023000api.fda.gov
Wilson-Cook Medical Inc.Winston Salem, NC, United StatesComplaint file establishment, Manufacturer2April 26, 2022000api.fda.gov
Applied Medical Resources Corp.Rsm, CA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer1March 18, 1992000api.fda.gov
Applied Medical Distribution CenterIrvine, CA, United StatesManufacturer1March 18, 1992000api.fda.gov
Endosound IncPortland, OR, United StatesComplaint file establishment, Manufacturer1October 17, 2025000api.fda.gov
Gyrus ACMI, Inc.Brooklyn Park, MN, United StatesComplaint file establishment, Specification developer1April 4, 2019000api.fda.gov
Centerpoint Systems LLCWest Valley City, UT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Nolato ContourBaldwin, WI, United StatesContract manufacturer0000api.fda.gov
OBP Medical CorporationLawrence, MA, United StatesSpecification developer0000api.fda.gov
PMC SMART Solutions, LLCShelbyville, IN, United StatesContract manufacturer0000api.fda.gov
Richard Wolf Medical Instruments Corp.Vernon Hills, IL, 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.