DeviceClearance

Product code GAD— General, Plastic Surgery

RETRACTOR

Classification name
Retractor
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
100
First cleared
Most recent

Market context for product code GAD

FDA has cleared 100 devices under product code GAD between 1976 and 2016, filed by 70 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 GAD

Adverse events under product code GAD

product code GAD
Malfunction
504
Total
504

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code GAD

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