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Data / Medical devices / Reminder, Medication / United States

FDA-registered makers of Reminder, Medication in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Reminder, Medication (product code NXQ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Get makers of this device in the United StatesWatch these makers
Device
Reminder, Medication
Product code
NXQ
Country
United States

Makers of Reminder, Medication in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Apothecary Products, LLC.Burnsville, MN, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
AdhereTechSummit, NJ, United StatesManufacturer0000api.fda.gov
Brightinsight Inc.San Jose, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dose Health, LLCMinneapolis, MN, United StatesSpecification developer0000api.fda.gov
Elvo Ai, Inc.West Bloomfield, MI, United StatesManufacturer0000api.fda.gov
Emocha Mobile Health Inc.Baltimore, MD, United StatesManufacturer0000api.fda.gov
Geri-Safe,ltd.Ithaca, NY, United StatesSpecification developer0000api.fda.gov
Hello HeartMenlo Park, CA, United StatesSpecification developer0000api.fda.gov
IV Ensure, IncDallas, TX, United StatesManufacturer, Specification developer0000api.fda.gov
Locked Brands LLC Dba MedsuresystemsRockwall, TX, United StatesManufacturer0000api.fda.gov
My Allergy Score, LLCFlorence, AL, United StatesManufacturer0000api.fda.gov
MedMinder Systems, Inc.Norwood, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Perigon Health 360 LLCPlymouth, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Rune Labs Inc.San Francisco, CA, United StatesManufacturer0000api.fda.gov
Rxcap Inc.Lynnfield, MA, United StatesSpecification developer0000api.fda.gov
Simplec, LLCMarietta, GA, United StatesManufacturer0000api.fda.gov
SMC, LLC.Nicholasville, KY, United StatesContract manufacturer0000api.fda.gov
Status Alert LLCRoswell, GA, United StatesSpecification developer0000api.fda.gov
Sequon, LLCAnnapolis, MD, United StatesSpecification developer0000api.fda.gov
Watchrx, Inc.Acton, MA, United StatesManufacturer0000api.fda.gov
WelldocColumbia, MD, United StatesManufacturer0000api.fda.gov
iPill IncRowland Heights, CA, United StatesManufacturer0000api.fda.gov
spencer Health SolutionsMorrisville, NC, United StatesSpecification developer0000api.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.