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Data / Medical devices / Cushion, Earphone (For Audiometric Testing) / United States

FDA-registered makers of Cushion, Earphone (For Audiometric Testing) in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Cushion, Earphone (For Audiometric Testing) (product code ETT). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Cushion, Earphone (For Audiometric Testing)
Product code
ETT
Country
United States

Makers of Cushion, Earphone (For Audiometric Testing) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arimon Technologies, Inc.Peshtigo, WI, United StatesContract manufacturer0000api.fda.gov
Etymotic Research, Inc.Schaumburg, IL, United StatesSpecification developer0000api.fda.gov
Gobiquity, Inc.Nashville, TN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Grason & Associates, LLCRindge, NH, United StatesManufacturer0000api.fda.gov
Hearing Lab Technology, LLCFort Worth, TX, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
JSM SolutionsFaribault, MN, United StatesSpecification developer0000api.fda.gov
R & D Medical Products, Inc.Lake Forest, CA, 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.