510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K855144Substantially Equivalent

Touriquet Kit with Snare

Dlp, Inc., Grand Rapids MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K855144 is the FDA 510(k) clearance record for TOURIQUET KIT WITH SNARE, a class I device, cleared for Dlp, Inc. on under FDA product code GDJ (Clamp, Surgical, General & Plastic Surgery). FDA records list 39 510(k) clearances for Dlp, Inc., from to . As of , FDA records show one recall naming K855144.

Clearance record

Decision date
Received
(41 days to decision)
Product code
GDJ Clamp, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Dlp, Inc. 620 Watson SW, Grand Rapids MI
Third party review
No

Clearances, product code GDJ

Trailing 12 months

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

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