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Data / Medical devices / Transducer, Ultrasonic / United States

FDA-registered makers of Transducer, Ultrasonic in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Transducer, Ultrasonic (product code JOP). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Transducer, Ultrasonic
Product code
JOP
Country
United States

Makers of Transducer, Ultrasonic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CorvascularMinnetonka, MN, United StatesManufacturer1July 19, 2024000api.fda.gov
US VascularBeaverton, OR, United StatesManufacturer1September 27, 2013000api.fda.gov
Cook IncorporatedEllettsville, IN, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer, Specification developer0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Natus Neurology IncorporatedMiddleton, WI, United StatesManufacturer0000api.fda.gov
Parks Medical Electronics, Inc.Aloha, OR, United StatesManufacturer0000api.fda.gov

Updated November 3, 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.