510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K110715Substantially Equivalent

Interdry Silver

Milliken Healthcare Products, LLC, Spartanburg SC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K110715 is the FDA 510(k) clearance record for INTERDRY SILVER, a class I device, cleared for Milliken Healthcare Products, LLC on under FDA product code FRL (Fiber, Medical, Absorbent). FDA records list 3 510(k) clearances for Milliken Healthcare Products, LLC, from to . As of , FDA records show no recalls naming K110715.

Clearance record

Decision date
Received
(234 days to decision)
Product code
FRL Fiber, Medical, Absorbent
Regulation
21 CFR 880.5300
Device class
Class I
Review panel
General Hospital
Applicant
Milliken Healthcare Products, LLC 920 Milliken Rd., Spartanburg SC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FRL

Trailing 12 months

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

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