510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K940036Substantially Equivalent

Endosurg Disposable Secondary Trocar

Endosurg, San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940036 is the FDA 510(k) clearance record for ENDOSURG DISPOSABLE SECONDARY TROCAR, a class II device, cleared for Endosurg on under FDA product code DRC (Trocar). FDA records list one 510(k) clearance for Endosurg. As of , FDA records show no recalls naming K940036.

Clearance record

Decision date
Received
(128 days to decision)
Product code
DRC Trocar
Regulation
21 CFR 870.1390
Device class
Class II
Review panel
Cardiovascular
Applicant
Endosurg 4227 Centergate, San Antonio TX
510(k) summary
Statement
Third party review
No

Clearances, product code DRC

Trailing 12 months

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

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