DeviceClearance

Product code HTD— General, Plastic Surgery

AALSTEAD MOSQ. FORCEPS, STRAIGHT, 5+SS 410 OR 420

Classification name
Forceps
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
73
First cleared
Most recent

Market context for product code HTD

FDA has cleared 73 devices under product code HTD between 1977 and 2005, filed by 25 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

Top applicants under product code HTD

Adverse events under product code HTD

product code HTD
Malfunction
892
Total
892

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 HTD

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