510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012957Substantially Equivalent

Towel Drape, Models 4409, 4410

Dynarex Corp., Maineville OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012957 is the FDA 510(k) clearance record for TOWEL DRAPE, MODELS 4409, 4410, a class II device, cleared for Dynarex Corp. on under FDA product code KKX (Drape, Surgical, Antimicrobial). FDA's definition for product code KKX reads: "Surgical drapes with an antimicrobial agent are subject to 510(k) review, under the procedures established by the 21st Century Cures Act. This product code is the class II non-exempt counterpart of PUI". FDA records list 27 510(k) clearances for Dynarex Corp., from to . As of , FDA records show no recalls naming K012957.

Clearance record

Decision date
Received
(183 days to decision)
Product code
KKX Drape, Surgical, Antimicrobial
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Dynarex Corp. 7736 Woodside Ct., Maineville OH
510(k) summary
Summary
Third party review
No

Clearances, product code KKX

Trailing 12 months

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

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