Product code LGF— Orthopedic

DELTA-LITE CASTING RESIN

Classification name
Component, Cast
Device class
Class 1
Regulation
21 CFR 888.5940
Advisory panel
Orthopedic
Total cleared
31
First cleared
Most recent

Market context for product code LGF

FDA has cleared 31 devices under product code LGF between 1978 and 2005, filed by 22 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 LGF

Recent clearances under product code LGF

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