510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K120012Substantially Equivalent

Integra Jarit Video Assisted Thoracic Surgery Instruments

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

K120012 is the FDA 510(k) clearance record for INTEGRA JARIT VIDEO ASSISTED THORACIC SURGERY INSTRUMENTS, a class II device, cleared for Integra LifeSciences Corporation on under FDA product code GCJ (Laparoscope, General & Plastic Surgery). FDA's definition for product code GCJ reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 94 510(k) clearances for Integra LifeSciences Corporation, from to . As of , FDA records show no recalls naming K120012.

Clearance record

Decision date
Received
(252 days to decision)
Product code
GCJ Laparoscope, General & Plastic Surgery
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Integra LifeSciences Corporation 589 Davies Dr., York PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GCJ

Trailing 12 months
27 clearances under product code GCJ in the twelve months to October 2026, February 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code GCJ, trailing twelve months
MonthClearances
November 20252
December 20250
January 20263
February 20264
March 20260
April 20263
May 20264
June 20264
July 20263
August 20262
September 20262
October 20260