510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925114Substantially Equivalent

Laparoscopic Instruments

Endo Technic Corp., Northbrook IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925114 is the FDA 510(k) clearance record for LAPAROSCOPIC INSTRUMENTS, a class II device, cleared for Endo Technic Corp. on under FDA product code HFI (Coagulator, Culdoscopic (And Accessories)). FDA records list 10 510(k) clearances for Endo Technic Corp., from to . As of , FDA records show no recalls naming K925114.

Clearance record

Decision date
Received
(507 days to decision)
Product code
HFI Coagulator, Culdoscopic (And Accessories)
Regulation
21 CFR 884.4160
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Endo Technic Corp. 3027 Commerical Ave., Northbrook IL
510(k) summary
Summary
Third party review
No

Clearances, product code HFI

Trailing 12 months

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

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