510(k) Report

FDA applicant

Perstorp AB C/O Robert Joel Slomoff

Potomac, MD2 decisions1987–19910 recalls

FDA records 2 decisions for Perstorp AB C/O Robert Joel Slomoff (Potomac, MD) from 1987 to 1991: 2 510(k) clearances. All are in product code KOZ (Beads, Hydrophilic, For Wound Exudate Absorption). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Perstorp AB C/O Robert Joel Slomoff’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perstorp AB C/O Robert Joel Slomoff since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Perstorp AB C/O Robert Joel Slomoff by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KOZBeads, Hydrophilic, For Wound Exudate Absorption2decisions

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K905069Iodosorb GelPerstorp AB C/O Robert Joel Slomoff · 19913cite it

What has FDA decided for it lately?

  • K905069Iodosorb GelPerstorp AB C/O Robert Joel Slomoff · 1991
  • K870559Iodosorb PowderPerstorp AB C/O Robert Joel Slomoff · 1987

All 2 as Perstorp AB C/O Robert Joel Slomoff →