DeviceClearance

Product code QUQ— General, Plastic Surgery

Kahook Dual Blade Glide (KDB Glide)

Classification name
Knife, Intraocular Pressure Lowering
Device class
Class 2
Regulation
21 CFR 878.4400
Advisory panel
General, Plastic Surgery
Total cleared
1
First cleared
Most recent

FDA classification definition

“A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma”

— U.S. Food and Drug Administration, device classification record for product code QUQ under 21 CFR 878.4400, via openFDA

Market context for product code QUQ

FDA has cleared 1 device under product code QUQ, all in 2024, filed by 1 applicant company. 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.

Top applicants under product code QUQ

Recent clearances under product code QUQ

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