510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923489Substantially Equivalent

Cox Disposable Retrieval Devices

Cox Medical Ent., Inc., Ventura CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923489 is the FDA 510(k) clearance record for COX DISPOSABLE RETRIEVAL DEVICES, a class II device, cleared for Cox Medical Ent., Inc. on under FDA product code OCZ (Endoscopic Grasping/Cutting Instrument, Non-Powered). FDA's definition for product code OCZ reads: "To manually grasp stones, tissues or other objects through an endoscope. To manipulate, sample or cut tissues through an endoscope". FDA records list 15 510(k) clearances for Cox Medical Ent., Inc., from to . As of , FDA records show no recalls naming K923489.

Clearance record

Decision date
Received
(70 days to decision)
Product code
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cox Medical Ent., Inc. 2186 Eastman Ave., Suite 110, Ventura CA
510(k) summary
Statement
Third party review
No

Clearances, product code OCZ

Trailing 12 months
1 clearance under product code OCZ in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OCZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260