DeviceClearance

Product code QPL— Neurology

Axon Therapy

Classification name
Electromagnetic Stimulator, Pain Relief
Device class
Class 2
Regulation
21 CFR 882.5890
Advisory panel
Neurology
Total cleared
6
First cleared
Most recent

FDA classification definition

“Intended to apply a magnetic-field induced electrical current to treat pain.”

— U.S. Food and Drug Administration, device classification record for product code QPL under 21 CFR 882.5890, via openFDA

Market context for product code QPL

FDA has cleared 6 devices under product code QPL between 2021 and 2025, filed by 5 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code QPL

Recent clearances under product code QPL

Data sourced from openFDA. This site is unofficial and independent of the FDA.