DeviceClearance

Product code KGE— Gastroenterology, Urology

Disposable Hot Biopsy Forceps

Classification name
Forceps, Biopsy, Electric
Device class
Class 2
Regulation
21 CFR 876.4300
Advisory panel
Gastroenterology, Urology
Total cleared
46
First cleared
Most recent

Market context for product code KGE

FDA has cleared 46 devices under product code KGE between 1989 and 2026, filed by 34 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code KGE

Recent clearances under product code KGE

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