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Data / Medical devices / System, Communication, Powered / United States

FDA-registered makers of System, Communication, Powered in the United States: 31 establishments

31 establishments in the United States are registered with the FDA to make System, Communication, Powered (product code ILQ). 0 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
System, Communication, Powered
Product code
ILQ
Country
United States

Makers of System, Communication, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ablenet, Inc.Roseville, MN, United StatesManufacturer0000api.fda.gov
Aionex, Inc.Madison, TN, United StatesManufacturer0000api.fda.gov
Anacom General CorporationAnaheim, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Austco Marketing & Service (usa) Ltd.Irving, TX, United StatesManufacturer0000api.fda.gov
Befitting You, LLCCommerce Twp, MI, United StatesSpecification developer0000api.fda.gov
Cadwell Industries, Inc.Kennewick, WA, United StatesSpecification developer0000api.fda.gov
Control Bionics Inc.Milford, OH, United StatesManufacturer, Specification developer0000api.fda.gov
Crest Electronics Inc.Dassel, MN, United StatesManufacturer0000api.fda.gov
Curbell Medical Products, Inc.Orchard Park, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Eyegaze Inc.Fairfax, VA, United StatesManufacturer0000api.fda.gov
Eyetech Digital SystemsTempe, AZ, United StatesSpecification developer0000api.fda.gov
Forbes Rehab Services Inc.Mansfield, OH, United StatesManufacturer0010api.fda.gov
Hatchmed CorporationKent, WA, United StatesManufacturer0000api.fda.gov
Hill-Rom, Inc.Raleigh, NC, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Intego Software, LLC D/B/A Critical AlertJacksonville, FL, United StatesManufacturer, Specification developer0000api.fda.gov
Jeron Electronic Systems IncNiles, IL, United StatesManufacturer0000api.fda.gov
KESTRA Medical Technologies, Inc.Kirkland, WA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Lingraphicare America, Inc.Princeton, NJ, United StatesManufacturer0000api.fda.gov
Med Labs, Inc.Goleta, CA, United StatesManufacturer0000api.fda.gov
MedMinder Systems, Inc.Norwood, MA, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Onyx Healthcare Usa, Inc.Orange, CA, United StatesManufacturer0000api.fda.gov
Prentke Romich CompanyWooster, OH, United StatesManufacturer0000api.fda.gov
Proxtalker.com LLCWaterbury, CT, United StatesManufacturer0000api.fda.gov
R & D Batteries, Inc.Burnsville, MN, United StatesManufacturer0000api.fda.gov
RCS Management CorporationSurprise, AZ, United StatesManufacturer0000api.fda.gov
Reliance Mobility LLCColumbia, TN, United StatesManufacturer0000api.fda.gov
S-Comm, Inc.Raytown, MO, United StatesSpecification developer0000api.fda.gov
Shelton Technologies And Resources LLCLakeland, FL, United StatesManufacturer0000api.fda.gov
Smartbox Assistive Technology IncLower Burrell, PA, United StatesManufacturer0000api.fda.gov
Smartbox UsCedar Falls, IA, United StatesManufacturer0000api.fda.gov
Tobii Dynavox LLCCoraopolis, PA, United StatesComplaint file establishment, Manufacturer, Specification developer0030api.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.