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
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| LifeSignals, Inc. | Milpitas, CA, United States | Complaint file establishment, Specification developer | 4 | July 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Sibel Health Inc. | Chicago, IL, United States | Manufacturer | 4 | June 3, 2024 | 0 | 0 | 0 | api.fda.gov |
| Biointellisense Inc. | Redwood City, CA, United States | Manufacturer, Specification developer | 3 | September 26, 2024 | 0 | 1 | 0 | api.fda.gov |
| Biointellisense Inc. | Golden, CO, United States | Manufacturer, Repackager or relabeler | 3 | September 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Carematix Inc. | Chicago, IL, United States | Manufacturer, Specification developer | 3 | May 5, 2010 | 0 | 0 | 0 | api.fda.gov |
| Scottcare Corporation | Cleveland, OH, United States | Manufacturer, Manufacturer for export | 2 | June 4, 2025 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical, Atrial Fibrillation Division, Inc. | Saint Paul, MN, United States | Manufacturer, Repackager or relabeler | 2 | December 20, 2013 | 0 | 0 | 0 | api.fda.gov |
| VitalConnect, Inc. | San Jose, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Reprocessor | 2 | April 20, 2020 | 0 | 1 | 0 | api.fda.gov |
| Boston Scientific Corporation | Maple Grove, MN, United States | Specification developer | 1 | March 24, 2017 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Saint Paul, MN, United States | Manufacturer | 1 | March 24, 2017 | 0 | 0 | 0 | api.fda.gov |
| Caretaker Medical | Charlottesville, VA, United States | Manufacturer, Specification developer | 1 | October 3, 2018 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 1 | June 21, 2006 | 0 | 0 | 0 | api.fda.gov |
| Cerner Corporation | Kansas City, MO, United States | Complaint file establishment, Manufacturer | 1 | November 27, 2009 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Westborough, MA, United States | Specification developer | 1 | June 21, 2006 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc | Salt Lake City, UT, United States | Specification developer | 1 | March 13, 2009 | 0 | 0 | 0 | api.fda.gov |
| LifeSync Corporation | Coral Springs, FL, United States | Specification developer | 1 | August 5, 2003 | 0 | 2 | 0 | api.fda.gov |
| Medicomp, Inc. | Melbourne, FL, United States | Specification developer | 1 | December 21, 2016 | 0 | 0 | 0 | api.fda.gov |
| Nihon Kohden America, Inc. | Irvine, CA, United States | Complaint file establishment, Manufacturer | 1 | June 29, 2007 | 0 | 1 | 0 | api.fda.gov |
| Nihon Kohden America Fulfillment Center | Foothill Ranch, CA, United States | Manufacturer | 1 | June 29, 2007 | 0 | 0 | 0 | api.fda.gov |
| Philips North America LLC | Cambridge, MA, United States | Complaint file establishment, Specification developer | 1 | April 16, 2020 | 0 | 0 | 0 | api.fda.gov |
| Solventum Us LLC | Eagan, MN, United States | Specification developer | 1 | May 3, 2012 | 0 | 0 | 0 | api.fda.gov |
| Solventum US LLC | San Antonio, TX, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | May 3, 2012 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical, Cardiology Division, Inc. | Plymouth, MN, United States | Complaint file establishment, Specification developer | 1 | October 21, 2011 | 0 | 0 | 0 | api.fda.gov |
| Vivalnk, Inc. | Campbell, CA, United States | Manufacturer, Specification developer | 1 | January 7, 2020 | 0 | 0 | 0 | api.fda.gov |
| All Quality & Services, Inc. | Fremont, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| All Quality & Services, Inc. | Garland, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Athena GTX | Johnston, IA, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Abbott Medical | Westford, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ActiGraph L.L.C. | Pensacola, FL, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caf Medical Solutions Inc | Hockley, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Creative Foam Corporation dba MT. OLIVE MFG | Mooresville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EDAN Diagnostics, Inc. | San Diego, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ever Ppe Inc | Sealy, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems Information Technologies | El Paso, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Medical Systems Information Technologies, Inc. | Waukesha, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Medical Systems Information Technologies, Inc. | Wauwatosa, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Happy Health | Austin, TX, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hinlab Inc. | Lewes, DE, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Katecho LLC | Des Moines, IA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MINDRAY DS USA, Inc. | Mahwah, NJ, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Metal Craft Machine & Engineering, Inc. | Elk River, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Murata Vios, Inc. | Woodbury, MN, United States | Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nortech Systems, Inc. | Milaca, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ontogen Manufacturing LLC | Lisle, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Andover, MA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Murrysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Riverside Machine & Engineering, Inc. | Eau Claire, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.