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Data / Medical devices / Coil, Magnetic Resonance, Specialty / United States

FDA-registered makers of Coil, Magnetic Resonance, Specialty in the United States: 25 establishments

25 establishments in the United States are registered with the FDA to make Coil, Magnetic Resonance, Specialty (product code MOS). 13 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Coil, Magnetic Resonance, Specialty
Product code
MOS
Country
United States

Makers of Coil, Magnetic Resonance, Specialty in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
GE Healthcare CoilsAurora, OH, United StatesManufacturer, Specification developer42January 23, 2026010api.fda.gov
Quality ElectrodynamicsMayfield Village, OH, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Manufacturer for export, Specification developer33February 28, 2025030api.fda.gov
Neocoil, LLCPewaukee, WI, United StatesComplaint file establishment, Contract manufacturer, Manufacturer17April 23, 2026020api.fda.gov
Ge Medical Systems, LLCWaukesha, WI, United StatesSpecification developer7April 1, 2011010api.fda.gov
Inkspace Imaging, IncPleasanton, CA, United StatesManufacturer6October 5, 2026000api.fda.gov
DXTX Medical Inc.Pittsburgh, PA, United StatesComplaint file establishment, Manufacturer5July 17, 2025000api.fda.gov
Polarean, Inc.Durham, NC, United StatesComplaint file establishment, Specification developer3November 19, 2024000api.fda.gov
ClearPoint Neuro Inc.Carlsbad, CA, United StatesManufacturer2September 8, 2011000api.fda.gov
Medspira LLCMinneapolis, MN, United StatesManufacturer2April 14, 2004000api.fda.gov
Monteris Medical CorpMinnetonka, MN, United StatesComplaint file establishment, Manufacturer2January 27, 2014000api.fda.gov
IMRIS Imaging, Inc.Chaska, MN, United StatesComplaint file establishment, Manufacturer1February 2, 2011000api.fda.gov
Nova Medical, IncWilmington, MA, United StatesContract manufacturer, Manufacturer1April 12, 2019000api.fda.gov
Scanmed, LLCOmaha, NE, United StatesManufacturer1December 5, 2014000api.fda.gov
Avnet, Inc. (Avnet Logistics)Chandler, AZ, United StatesContract manufacturer0000api.fda.gov
Benchmark Electronics, Inc.Nashua, NH, United StatesContract manufacturer0000api.fda.gov
Creative Foam Corporation - BremenBremen, IN, United StatesContract manufacturer0000api.fda.gov
Evolve Manufacturing Technologies Inc.Fremont, CA, United StatesContract manufacturer0000api.fda.gov
GE Healthcare Manufacturing LLCFlorence, SC, United StatesManufacturer0000api.fda.gov
GE Healthcare Manufacturing LLCFlorence, SC, United StatesManufacturer0000api.fda.gov
HM Product Solutions, Ltd.Hartland, WI, United StatesContract manufacturer0000api.fda.gov
Haywood Vocational Opportunities Inc.Waynesville, NC, United StatesContract manufacturer0000api.fda.gov
Hyperfine, IncGuilford, CT, United StatesManufacturer0000api.fda.gov
Promaxo, LLCOakland, CA, United StatesSpecification developer0000api.fda.gov
Steripack Usa (limited) LLCLakeland, FL, United StatesContract manufacturer0000api.fda.gov
Uih Technologies, LLCHouston, TX, 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.