Product code KDD— General, Plastic Surgery

STERILE SUTURE REMOVAL KIT

Classification name
Kit, Surgical Instrument, Disposable
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
62
First cleared
Most recent

Market context for product code KDD

FDA has cleared 62 devices under product code KDD between 1976 and 2008, filed by 51 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 KDD

Recent clearances under product code KDD

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