DeviceClearance

Product code GES— General, Plastic Surgery

SURGICAL BLADES

Classification name
Blade, Scalpel
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
48
First cleared
Most recent

Market context for product code GES

FDA has cleared 48 devices under product code GES between 1976 and 2003, filed by 37 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

last 15 years

Top applicants under product code GES

Recent clearances under product code GES

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