DeviceClearance

Product code EGJ— Physical Medicine

ACTHYDERM

Classification name
Device, Iontophoresis, Other Uses
Device class
Class 2
Regulation
21 CFR 890.5525
Advisory panel
Physical Medicine
Total cleared
73
First cleared
Most recent

Market context for product code EGJ

FDA has cleared 73 devices under product code EGJ between 1977 and 2025, filed by 40 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

last 15 years

Top applicants under product code EGJ

Recent clearances under product code EGJ

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