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
K914365Substantially Equivalent

Dexon Dissecting Sponge

Davis & Geck, Inc., Danbury CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914365 is the FDA 510(k) clearance record for DEXON DISSECTING SPONGE, a class II device, cleared for Davis & Geck, Inc. on under FDA product code GAK (Suture, Absorbable). FDA records list 45 510(k) clearances for Davis & Geck, Inc., from to . As of , FDA records show no recalls naming K914365.

Clearance record

Decision date
Received
(22 days to decision)
Product code
GAK Suture, Absorbable
Regulation
21 CFR 878.4830
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Davis & Geck, Inc. American Cynamid Company, Danbury CT
510(k) summary
Statement
Third party review
No

Clearances, product code GAK

Trailing 12 months

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

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