Acryderm Gel Wound Dressing

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

510(k) Number

K970693 ↗

FDA Product Code

MGQ

Device Class

U

Advisory Committee

Unknown

FDA Decision

SN

• Acry Island Border Dressing, Models 2031, 2032, 2033

  Class I

  FDA 510(k) K992032 Active Cleared 19 Aug 1999

• Acryderm Silver Anttimicrobial Wound Gel Model# A-002101

  Unclassified

  FDA 510(k) K011994 Active Cleared 8 Nov 2001

• Acryderm Silver Antimicrobial Otc Wound Gel

  Unclassified

  FDA 510(k) K070333 Active Cleared 10 Jul 2007

• Acrynoodles Absorbent Wound Dressing

  Unclassified

  FDA 510(k) K962851 Active Cleared 6 Sep 1996

• Acryderm Silver Anti-Microbial Wound Dressing, Models 1041, 1042, 1043, 1044, 1045

  Unclassified

  FDA 510(k) K991818 Active Cleared 17 Apr 2000

• Acryderm Antimicrobial Silver Gel Wound Dressing Model #b

  Unclassified

  FDA 510(k) K083103 Active Cleared 26 Feb 2009

See all devices from Acrymed, Inc. →