510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K942815Substantially Equivalent for Some Indications

Hydroskin Wound Dressing

Hymedix Intl., Inc., Dayton NJ / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K942815 is the FDA 510(k) clearance record for HYDROSKIN WOUND DRESSING, a class I device, cleared for Hymedix Intl., Inc. on under FDA product code KMF (Bandage, Liquid). FDA records list 2 510(k) clearances for Hymedix Intl., Inc., from to . As of , FDA records show no recalls naming K942815.

Clearance record

Decision date
Received
(26 days to decision)
Product code
KMF Bandage, Liquid
Regulation
21 CFR 880.5090
Device class
Class I
Review panel
General Hospital
Applicant
Hymedix Intl., Inc. 2235 Rte. 130, Dayton NJ
Third party review
No

Clearances, product code KMF

Trailing 12 months

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

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