510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K905069Substantially Equivalent

Iodosorb Gel

Perstorp AB C/O Robert Joel Slomoff, Potomac MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905069 is the FDA 510(k) clearance record for IODOSORB GEL, a class I device, cleared for Perstorp AB C/O Robert Joel Slomoff on under FDA product code KOZ (Beads, Hydrophilic, For Wound Exudate Absorption). FDA records list 2 510(k) clearances for Perstorp AB C/O Robert Joel Slomoff, from to . As of , FDA records show no recalls naming K905069.

Clearance record

Decision date
Received
(83 days to decision)
Product code
KOZ Beads, Hydrophilic, For Wound Exudate Absorption
Regulation
21 CFR 878.4018
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Perstorp AB C/O Robert Joel Slomoff 9229 Cranford Dr., Potomac MD
Third party review
No

Clearances, product code KOZ

Trailing 12 months

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

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