DeviceClearance

Product code GAA— General, Plastic Surgery

14 INCH BULLET POINT NEEDLE

Classification name
Needle, Aspiration And Injection, Disposable
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
107
First cleared
Most recent

Market context for product code GAA

FDA has cleared 107 devices under product code GAA between 1976 and 2023, filed by 63 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 GAA

Adverse events under product code GAA

product code GAA
Malfunction
834
Total
834

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 GAA

1–100 of 107

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