Skip to content

Iodosorb Powder

by Perstorp AB C/O Robert Joel Slomoff

510(k) K870559

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK870559 Date20 Mar 1987DecidedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
KOZ
Device Class
Class I
Regulation
21 CFR Part 878.4018
Advisory Committee
General, Plastic Surgery
FDA Decision
SN

Other devices from Perstorp AB C/O Robert Joel Slomoff

  • Iodosorb Gel

    Class I