Product code MNE— Physical Medicine

PODIATRIC MATERIAL

Classification name
Orthosis, Moldable, Supportive, Skin Protective
Device class
Class 1
Regulation
21 CFR 890.3475
Advisory panel
Physical Medicine
Total cleared
2
First cleared
Most recent

Market context for product code MNE

FDA has cleared 2 devices under product code MNE between 1978 and 1994, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

Top applicants under product code MNE

Recent clearances under product code MNE

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