DeviceClearance

Product code HMP— General, Plastic Surgery

EYE PAD

Classification name
Pad, Eye
Device class
Class 1
Regulation
21 CFR 878.4440
Advisory panel
General, Plastic Surgery
Total cleared
17
First cleared
Most recent

Market context for product code HMP

FDA has cleared 17 devices under product code HMP between 1978 and 1994, filed by 16 applicant companies. 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 HMP

Recent clearances under product code HMP

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