Micronet Light Dressing Sponge

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K780408 ↗

FDA Product Code

NAB

Device Class

Class I

Regulation

21 CFR Part 878.4014

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Conform Stretch Bandage (5SIZES)

  Class I

  FDA 510(k) K771452 Active Cleared 12 Sep 1977

• Sponge, Curity Washed Gauze

  Class I

  FDA 510(k) K760094 Active Cleared 16 Jul 1976

• Urine Specimen Collecting Device

  Class II

  FDA 510(k) K772133 Active Cleared 28 Nov 1977

• T.E.D. Sequential Compression Sleeves

  Class II

  FDA 510(k) K781357 Active Cleared 20 Sep 1978

• Tender-Sorb Drain Sponges

  Class I

  FDA 510(k) K802225 Active Cleared 26 Sep 1980

• Curity Peakometer

  Class II

  FDA 510(k) K771655 Active Cleared 14 Oct 1977

See all devices from Kendall Research Center →