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Data / Medical devices / Device, Incontinence, Mechanical/Hydraulic

Device, Incontinence, Mechanical/Hydraulic (EZY): 4 FDA-registered makers in 1 country

4 establishments in 1 country are registered with the FDA to make Device, Incontinence, Mechanical/Hydraulic (product code EZY, Class 3, 21 CFR 876.5280). 3 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 5 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
EZY
Device class
3
Regulation
876.5280
Medical specialty
Gastroenterology, Urology
Implant
Yes

Makers by country

CountryMakers
United States4

Makers of Device, Incontinence, Mechanical/Hydraulic

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
Boston Scientific CorporationMarlborough, MA, United StatesSpecification developer0120api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesComplaint file establishment, Manufacturer0100api.fda.gov
Uromedica, Inc.Plymouth, MN, United StatesManufacturer0110api.fda.gov
Sterigenics US LLCGurnee, IL, United StatesContract sterilizer, Manufacturer for export0000api.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.