Product code GFE— General, Plastic Surgery
DERMABRADER
- Classification name
- Brush, Dermabrasion, Powered
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code GFE
FDA has cleared devices under product code GFE between 1990 and 1996, filed by 2 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
- 1996
- 1990
Top applicants under product code GFE
Recent clearances under product code GFE
Data sourced from openFDA. This site is unofficial and independent of the FDA.