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Data / Medical devices / Transformer, Endoscope

Transformer, Endoscope (GCW): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Transformer, Endoscope (product code GCW, Class 2, 21 CFR 876.1500). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on November 22, 1977, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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

Makers by country

CountryMakers
Japan2
United States1
China1

Makers of Transformer, 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
Welch Allyn, Inc.Skaneateles Falls, NY, United StatesManufacturer1November 22, 1977000api.fda.gov
Olympus Medical Systems Corp.HACHIOJI-SHI Tokyo, JapanSpecification developer0000api.fda.gov
Shirakawa Olympus Co., Ltd.NISHISHIRAKAWA-GUN Fukushima, JapanManufacturer0000api.fda.gov
Suzhou Shangchuang Technology Service Co., Ltd.Suzhou Jiangsu, ChinaManufacturer0000api.fda.gov

Updated November 22, 1977. 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.