Gauze Compress

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K960615 ↗

FDA Product Code

EFQ

Device Class

U

Advisory Committee

Unknown

FDA Decision

SN

• Certiburn Burn/Trauma Face Dressing /Towel Dressing

  Not classified

  FDA 510(k) K940249 Active Cleared 3 Oct 1994

• X-Large Multi-Function Trauma Dressing

  Unclassified

  FDA 510(k) K940358 Active Cleared 23 Mar 1994

• 2, 3 & 4 Bandadge Compress

  Unclassified

  FDA 510(k) K945004 Active Cleared 22 Mar 1995

• Certiburn Burn/Trauma Face Dressing, Towel Dressing

  Unclassified

  FDA 510(k) K946338 Active Cleared 29 Mar 1995

• Triangular Bandage

  Unclassified

  FDA 510(k) K940345 Active Cleared 25 Feb 1994

• Cprotector

  Class II

  FDA 510(k) K934821 Active Cleared 6 Jan 1994

See all devices from Certified Safety Mfg., Inc. →