DeviceClearance

Product code GEN— General, Plastic Surgery

FORCEPS

Classification name
Forceps, General & Plastic Surgery
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
104
First cleared
Most recent

Market context for product code GEN

FDA has cleared 104 devices under product code GEN between 1976 and 2003, filed by 57 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 GEN

Recent clearances under product code GEN

1–100 of 104

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