510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220891Substantially Equivalent

Kahook Dual Blade Glide (KDB Glide)

New World Medical, Inc., Rancho Cucamonga CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220891 is the FDA 510(k) clearance record for Kahook Dual Blade Glide (KDB Glide), a class II device, cleared for New World Medical, Inc. on under FDA product code QUQ (Knife, Intraocular Pressure Lowering). FDA's definition for product code QUQ reads: "A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma". FDA records list 12 510(k) clearances for New World Medical, Inc., from to . As of , FDA records show no recalls naming K220891.

Clearance record

Decision date
Received
(781 days to decision)
Product code
QUQ Knife, Intraocular Pressure Lowering
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
New World Medical, Inc. 10763 Edison Ct., Rancho Cucamonga CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QUQ

Trailing 12 months

FDA records hold no clearances under product code QUQ in the trailing twelve months.

FDA records show no clearances under product code QUQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code QUQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260