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Data / Medical devices / Transmitters And Receivers, Electrocardiograph, Telephone / United States

FDA-registered makers of Transmitters And Receivers, Electrocardiograph, Telephone in the United States: 31 establishments

31 establishments in the United States are registered with the FDA to make Transmitters And Receivers, Electrocardiograph, Telephone (product code DXH). 12 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.

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Device
Transmitters And Receivers, Electrocardiograph, Telephone
Product code
DXH
Country
United States

Makers of Transmitters And Receivers, Electrocardiograph, Telephone in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
AliveCorMountain View, CA, United StatesComplaint file establishment, Manufacturer, Specification developer10May 25, 2022010api.fda.gov
TZ Medical, Inc.Tualatin, OR, United StatesManufacturer, Specification developer4December 21, 2000000api.fda.gov
Philips North America LLCCambridge, MA, United StatesComplaint file establishment, Specification developer2September 21, 2000000api.fda.gov
RR Donnelley-Supply Chain SolutionsPlover, WI, United StatesContract manufacturer, Repackager or relabeler2November 30, 2021000api.fda.gov
Scottcare CorporationCleveland, OH, United StatesManufacturer2September 15, 2006000api.fda.gov
BiotricityRedwood City, CA, United StatesManufacturer1December 15, 2017000api.fda.gov
Datrix LLCEscondido, CA, United StatesSpecification developer1August 12, 2004000api.fda.gov
HeartbeamSanta Clara, CA, United StatesManufacturer1December 8, 2025000api.fda.gov
Lohman Technologies, LLCPewaukee, WI, United StatesManufacturer1June 23, 2006000api.fda.gov
Philips North America LLCAndover, MA, United StatesSpecification developer1November 7, 1991000api.fda.gov
RhythmedixMount Laurel, NJ, United StatesComplaint file establishment, Manufacturer, Specification developer1August 5, 2014000api.fda.gov
VivaQuant, IncArden Hills, MN, United StatesManufacturer1February 16, 2019000api.fda.gov
Abbott MedicalSylmar, CA, United StatesManufacturer0000api.fda.gov
Advanced Monitored CaregivingNew York, NY, United StatesManufacturer0000api.fda.gov
Analog DevicesWilmington, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov
GE Medical Systems Information Technologies, Inc.Waukesha, WI, United StatesSpecification developer0000api.fda.gov
GE Medical Systems Information Technologies, Inc.Wauwatosa, WI, United StatesManufacturer, Specification developer0000api.fda.gov
Global Instrumentation, LLCE Syracuse, NY, United StatesManufacturer0000api.fda.gov
Irhythm Technologies, Inc.San Francisco, CA, United StatesSpecification developer0000api.fda.gov
KESTRA Medical Technologies, Inc.Kirkland, WA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Kitron Technologies Inc.Windber, PA, United StatesContract manufacturer0000api.fda.gov
LifeSignals, Inc.Milpitas, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Masimo CorporationIrvine, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Medtronic, Inc.Mounds View, MN, United StatesManufacturer0000api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
NextPhase Medical Devices, LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
Philips North America LLCMurrysville, PA, United StatesContract manufacturer0000api.fda.gov
Spacelabs Healthcare Inc.Snoqualmie, WA, United StatesContract manufacturer0010api.fda.gov
Twin River GroupTrenton, NJ, United StatesManufacturer0000api.fda.gov
iRhythm Technologies, Inc.Cypress, CA, 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.