510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K103726Substantially Equivalent

Jarit Take-Apart Endoscopic Instruments

Integra LifeSciences Corporation, York PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K103726 is the FDA 510(k) clearance record for JARIT TAKE-APART ENDOSCOPIC INSTRUMENTS, a class II device, cleared for Integra LifeSciences Corporation on under FDA product code KNF (Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)). FDA records list 94 510(k) clearances for Integra LifeSciences Corporation, from to . As of , FDA records show one recall naming K103726.

Clearance record

Decision date
Received
(413 days to decision)
Product code
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Regulation
21 CFR 884.4160
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Integra LifeSciences Corporation 589 Davies Dr., York PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KNF

Trailing 12 months
1 clearance under product code KNF in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KNF, 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 20261
October 20260