DeviceClearance

Product code NFO— Neurology

2 Face / Face Evolution

Classification name
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Device class
Class 2
Regulation
21 CFR 882.5890
Advisory panel
Neurology
Total cleared
81
First cleared
Most recent

Market context for product code NFO

FDA has cleared 81 devices under product code NFO between 2001 and 2026, filed by 60 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 NFO

Recent clearances under product code NFO

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