510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023688Substantially Equivalent

Lemaitre Vascular Disposable Vein Stripper

LeMaitre Vascular Inc., Burlington MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K023688 is the FDA 510(k) clearance record for LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER, a class I device, cleared for LeMaitre Vascular, Inc. on under FDA product code GAF (Spatula, Surgical, General & Plastic Surgery). FDA records list 35 510(k) clearances for LeMaitre Vascular, Inc., from to . As of , FDA records show no recalls naming K023688.

Clearance record

Decision date
Received
(90 days to decision)
Product code
GAF Spatula, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
LeMaitre Vascular, Inc. 26 Ray Ave., Burlington MA
510(k) summary
Statement
Third party review
No

Clearances, product code GAF

Trailing 12 months

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

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