Data / Medical devices / United States / Remedy Logic, Inc

Remedy Logic, Inc: FDA-registered device maker in New York, NY, United States, 1 510(k) clearance

Remedy Logic, Inc is registered with the FDA (registration 3042852277) in New York, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 30, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3042852277

Address

6 Saint Johns Ln, New York, NY, United States, 10013

Owner or operator

Remedy Logic, Inc (10094872)

Roles

Manufacturer, Specification developer

First device listed

December 30, 2025

Registered through

2026

Brand names listed

RemedyLogic AI MRI Lumbar Spine Reader

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

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Updated October 30, 2024. 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.