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Data / Medical devices / Stethoscope, Electronic / United States

FDA-registered makers of Stethoscope, Electronic in the United States: 17 establishments

17 establishments in the United States are registered with the FDA to make Stethoscope, Electronic (product code DQD). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.

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Device
Stethoscope, Electronic
Product code
DQD
Country
United States

Makers of Stethoscope, Electronic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Eko Health, Inc.Emeryville, CA, United StatesComplaint file establishment, Manufacturer, Specification developer7July 23, 2026000api.fda.gov
American Diagnostic Corp.Hauppauge, NY, United StatesManufacturer, Repackager or relabeler2March 10, 2017000api.fda.gov
Medaica IncHenderson, NV, United StatesSpecification developer1January 19, 2023000api.fda.gov
Neko Health Manufacturing LLCEnglewood, CO, United StatesManufacturer1November 26, 2003000api.fda.gov
Solventum Us LLCEagan, MN, United StatesSpecification developer1February 22, 2005000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Specification developer1February 22, 2005000api.fda.gov
Zien Medical Technologies LLCSalt Lake City, UT, United StatesSpecification developer1August 4, 2021000api.fda.gov
All Quality & Services, Inc.Fremont, CA, United StatesContract manufacturer0000api.fda.gov
All Quality & Services, Inc.Garland, TX, United StatesContract manufacturer0000api.fda.gov
Analog DevicesWilmington, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dictum Health, Inc.Malibu, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Echonous, Inc.Redmond, WA, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
East West WisconsinWhitewater, WI, United StatesContract manufacturer0000api.fda.gov
Medwand Solutions, IncRsm, CA, United StatesSpecification developer0000api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
NextPhase Medical Devices, LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
Solventum US LLCColumbia, MO, 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.