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
K925559Substantially Equivalent

Biliary Stone Dislodger

Annex Medical, Inc., Eden Prairie MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925559 is the FDA 510(k) clearance record for BILIARY STONE DISLODGER, a class II device, cleared for Annex Medical, Inc. on under FDA product code LQR (Dislodger, Stone, Biliary). FDA records list 23 510(k) clearances for Annex Medical, Inc., from to . As of , FDA records show no recalls naming K925559.

Clearance record

Decision date
Received
(44 days to decision)
Product code
LQR Dislodger, Stone, Biliary
Regulation
21 CFR 876.5010
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Annex Medical, Inc. 7887 Fuller Rd. #109, Eden Prairie MN
510(k) summary
Summary
Third party review
No

Clearances, product code LQR

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