510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K232370Substantially Equivalent

Percutaneous Nephroscope System

Karl Storz SE & Co. KG, Tuttlingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232370 is the FDA 510(k) clearance record for Percutaneous Nephroscope System, a class II device, cleared for Karl Storz SE & CO. KG on under FDA product code FGA (Kit, Nephroscope). FDA records list 26 510(k) clearances for Karl Storz SE & CO. KG, from to . As of , FDA records show 8 recalls naming K232370.

Clearance record

Decision date
Received
(267 days to decision)
Product code
FGA Kit, Nephroscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Karl Storz SE & CO. KG Dr.-Karl-Storz-Straße 34, Tuttlingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FGA

Trailing 12 months

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

FDA records show no clearances under product code FGA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FGA, 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