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Data / Medical devices / Transmitters And Receivers, Physiological Signal, Radiofrequency / United States

FDA-registered makers of Transmitters And Receivers, Physiological Signal, Radiofrequency in the United States: 47 establishments

47 establishments in the United States are registered with the FDA to make Transmitters And Receivers, Physiological Signal, Radiofrequency (product code DRG). 24 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.

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Device
Transmitters And Receivers, Physiological Signal, Radiofrequency
Product code
DRG
Country
United States

Makers of Transmitters And Receivers, Physiological Signal, Radiofrequency in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
LifeSignals, Inc.Milpitas, CA, United StatesComplaint file establishment, Specification developer4July 9, 2026000api.fda.gov
Sibel Health Inc.Chicago, IL, United StatesManufacturer4June 3, 2024000api.fda.gov
Biointellisense Inc.Redwood City, CA, United StatesManufacturer, Specification developer3September 26, 2024010api.fda.gov
Biointellisense Inc.Golden, CO, United StatesManufacturer, Repackager or relabeler3September 26, 2024000api.fda.gov
Carematix Inc.Chicago, IL, United StatesManufacturer, Specification developer3May 5, 2010000api.fda.gov
Scottcare CorporationCleveland, OH, United StatesManufacturer, Manufacturer for export2June 4, 2025000api.fda.gov
St. Jude Medical, Atrial Fibrillation Division, Inc.Saint Paul, MN, United StatesManufacturer, Repackager or relabeler2December 20, 2013000api.fda.gov
VitalConnect, Inc.San Jose, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Reprocessor2April 20, 2020010api.fda.gov
Boston Scientific CorporationMaple Grove, MN, United StatesSpecification developer1March 24, 2017000api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesManufacturer1March 24, 2017000api.fda.gov
Caretaker MedicalCharlottesville, VA, United StatesManufacturer, Specification developer1October 3, 2018000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer1June 21, 2006000api.fda.gov
Cerner CorporationKansas City, MO, United StatesComplaint file establishment, Manufacturer1November 27, 2009000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer1June 21, 2006000api.fda.gov
Icu Medical, IncSalt Lake City, UT, United StatesSpecification developer1March 13, 2009000api.fda.gov
LifeSync CorporationCoral Springs, FL, United StatesSpecification developer1August 5, 2003020api.fda.gov
Medicomp, Inc.Melbourne, FL, United StatesSpecification developer1December 21, 2016000api.fda.gov
Nihon Kohden America, Inc.Irvine, CA, United StatesComplaint file establishment, Manufacturer1June 29, 2007010api.fda.gov
Nihon Kohden America Fulfillment CenterFoothill Ranch, CA, United StatesManufacturer1June 29, 2007000api.fda.gov
Philips North America LLCCambridge, MA, United StatesComplaint file establishment, Specification developer1April 16, 2020000api.fda.gov
Solventum Us LLCEagan, MN, United StatesSpecification developer1May 3, 2012000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Manufacturer, Specification developer1May 3, 2012000api.fda.gov
St. Jude Medical, Cardiology Division, Inc.Plymouth, MN, United StatesComplaint file establishment, Specification developer1October 21, 2011000api.fda.gov
Vivalnk, Inc.Campbell, CA, United StatesManufacturer, Specification developer1January 7, 2020000api.fda.gov
All Quality & Services, Inc.Fremont, CA, United StatesContract manufacturer0000api.fda.gov
All Quality & Services, Inc.Garland, TX, United StatesContract manufacturer0000api.fda.gov
Athena GTXJohnston, IA, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
Abbott MedicalWestford, MA, United StatesSpecification developer0000api.fda.gov
ActiGraph L.L.C.Pensacola, FL, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Caf Medical Solutions IncHockley, TX, United StatesManufacturer0000api.fda.gov
Creative Foam Corporation dba MT. OLIVE MFGMooresville, IN, United StatesContract manufacturer0000api.fda.gov
EDAN Diagnostics, Inc.San Diego, CA, United StatesContract manufacturer0000api.fda.gov
Ever Ppe IncSealy, TX, United StatesContract manufacturer0000api.fda.gov
Ge Medical Systems Information TechnologiesEl Paso, TX, United StatesManufacturer0000api.fda.gov
GE Medical Systems Information Technologies, Inc.Waukesha, WI, United StatesSpecification developer0000api.fda.gov
GE Medical Systems Information Technologies, Inc.Wauwatosa, WI, United StatesSpecification developer0000api.fda.gov
Happy HealthAustin, TX, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Hinlab Inc.Lewes, DE, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Katecho LLCDes Moines, IA, United StatesContract manufacturer0000api.fda.gov
MINDRAY DS USA, Inc.Mahwah, NJ, United StatesComplaint file establishment, Contract manufacturer0000api.fda.gov
Metal Craft Machine & Engineering, Inc.Elk River, MN, United StatesContract manufacturer0000api.fda.gov
Murata Vios, Inc.Woodbury, MN, United StatesComplaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Nortech Systems, Inc.Milaca, MN, United StatesContract manufacturer0000api.fda.gov
Ontogen Manufacturing LLCLisle, IL, United StatesContract manufacturer0000api.fda.gov
Philips North America LLCAndover, MA, United StatesManufacturer, Specification developer0000api.fda.gov
Philips North America LLCMurrysville, PA, United StatesContract manufacturer0000api.fda.gov
Riverside Machine & Engineering, Inc.Eau Claire, WI, United StatesContract manufacturer0000api.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.