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Data / Medical devices / Accessories, Cleaning, For Endoscope

Accessories, Cleaning, For Endoscope (FEB): 18 FDA-registered makers in 4 countries

18 establishments in 4 countries are registered with the FDA to make Accessories, Cleaning, For Endoscope (product code FEB, Class 2, 21 CFR 876.1500). 15 of them have a 510(k) clearance or PMA approval on file and 5 have a recall event. The FDA has issued 58 510(k) clearances under this code, the latest on October 2, 2026, and lists 20 recall events (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
FEB
Device class
2
Regulation
876.1500
Medical specialty
Gastroenterology, Urology

Makers by country

CountryMakers
United States14
Japan2
Mexico1
China1

Makers of Accessories, Cleaning, For Endoscope

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medivators IncMinneapolis, MN, United StatesComplaint file establishment, Manufacturer, Manufacturer for export, Specification developer8October 2, 2026010api.fda.gov
Advanced Sterilization ProductsIrvine, CA, United StatesComplaint file establishment, Specification developer4April 23, 2019060api.fda.gov
Aizu Olympus Co., Ltd.AIZUWAKAMATSU-SHI Fukushima, JapanManufacturer4September 1, 2020010api.fda.gov
Olympus Medical Systems Corp.HACHIOJI-SHI Tokyo, JapanSpecification developer4September 1, 2020000api.fda.gov
STERIS CorporationMentor, OH, United StatesManufacturer, Repackager or relabeler3October 2, 2026000api.fda.gov
Wassenburg Medical, Inc.Ivyland, PA, United StatesManufacturer3December 19, 2024010api.fda.gov
Medivators IncConroe, TX, United StatesManufacturer2January 14, 2022000api.fda.gov
Steris CorporationMentor, OH, United StatesSpecification developer2December 2, 2024040api.fda.gov
STERIS CorporationMentor, OH, United StatesManufacturer2December 2, 2024000api.fda.gov
CovidienTIJUANA, B.C. Mexico, MexicoContract manufacturer, Manufacturer1September 20, 1994000api.fda.gov
CovidienNorth Haven, CT, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer1September 20, 1994000api.fda.gov
CovidienPonce, PR, United StatesContract manufacturer, Manufacturer1September 20, 1994000api.fda.gov
Hobbs Medical, Inc.Stafford Springs, CT, United StatesContract manufacturer, Manufacturer1October 28, 1993000api.fda.gov
Steris CorporationSaint Louis, MO, United StatesManufacturer1October 2, 2026000api.fda.gov
TeleMed SystemsNorthborough, MA, United StatesSpecification developer1June 11, 1990000api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer for export0000api.fda.gov
Jabil Inc.Auburn Hills, MI, United StatesContract manufacturer0000api.fda.gov
Saint-Gobain Life Sciences (Hangzhou) Co., LtdHangzhou Zhejiang, ChinaContract manufacturer0000api.fda.gov

Updated October 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.