510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924117Unknown

Dexide Laparoscopic Kits

Dexide, Inc., Fort Worth TX / Traditional, Unknown
FDA source (opens on fda.gov)

K924117 is the FDA 510(k) clearance record for DEXIDE LAPAROSCOPIC KITS, a class I device, cleared for Dexide, Inc. on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 38 510(k) clearances for Dexide, Inc., from to . As of , FDA records show no recalls naming K924117.

Clearance record

Decision date
Received
(221 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Dexide, Inc. 7509 Flagstone Dr., Fort Worth TX
510(k) summary
Statement
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

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