Tecnol Variable Tension Bandage

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K884440 ↗

FDA Product Code

NAD

Device Class

Class I

Regulation

21 CFR Part 878.4020

Advisory Committee

General, Plastic Surgery

FDA Decision

SN

• Bedpan, Single Patient Use, Tecnol

  Class I

  FDA 510(k) K760307 Active Cleared 11 Aug 1976

• I.V. Support, Tecnol Armboard

  Class I

  FDA 510(k) K760308 Active Cleared 11 Aug 1976

• Tecnol Fog-Free Surgical Mask W/Derma-Touch Tape

  Class II

  FDA 510(k) K873785 Active Cleared 2 Nov 1987

• Tecnol Compression Knee Dressing

  Class II

  FDA 510(k) K873368 Active Cleared 11 Dec 1987

• Tecnol Patient Use Ice Pack

  Class II

  FDA 510(k) K760782 Active Cleared 2 Dec 1976

• Disposable Abdominal Binder

  Class I

  FDA 510(k) K760772 Active Cleared 3 Nov 1976

See all devices from Tecnol New Jersey Wound Care, Inc. →