Oasis Dry Mouth Relief Discs or Oasis Mouth Moisturizing Discs

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

510(k) Number

K041563 ↗

FDA Product Code

LFD

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Biotene Moisturizing Mouth Spray for Dry Mouth Symptom Relief

  Unclassified

  FDA 510(k) K103745 Active Cleared 20 Jul 2011

• Actiprotect Uc N95 Respirator

  Class II

  FDA 510(k) K093189 Active Cleared 2 Jul 2010

• Biotene Oral Balance Gel, Biotene Dry Mouth Oral Rinse, Biotene Moisturizing Mouth Spray

  Unclassified

  FDA 510(k) K123731 Active Cleared 4 Jan 2013

• Biotene Dry Mouth Mouthwash, Biotene Pbf Dry Mouth Mouthwash

  Unclassified

  FDA 510(k) K101477 Active Cleared 28 Sep 2010

• Actiprotect Uf N95 Respirator, Double Strap, Flat Fold

  Class II

  FDA 510(k) K081923 Active Cleared 1 Jul 2009

• Actiprotect Uf N95 Respirator

  Class II

  FDA 510(k) K093161 Active Cleared 10 May 2010