DeviceClearance

Product code NAD— General, Plastic Surgery

2018 ARTERIAL/VENOUS PRESSURE DRESSING

Classification name
Dressing, Wound, Occlusive
Device class
Class 1
Regulation
21 CFR 878.4020
Advisory panel
General, Plastic Surgery
Total cleared
108
First cleared
Most recent

Market context for product code NAD

FDA has cleared 108 devices under product code NAD between 1977 and 2026, filed by 77 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 NAD

Adverse events under product code NAD

product code NAD
Injury
431
Malfunction
11,935
Other
1
Total
12,367

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 NAD

1–100 of 108

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