FDA Device Intelligence
HomeDevice types › KXF

Applicator, Absorbent Tipped, Non-Sterile

FDA product code KXF · Class 1 · General Hospital

352
Registered devices
552
Adverse events
2
Recalls
21
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-02-03Avanos Medical, Inc.Incorrect expiration date.
2013-03-26Owens & Minor Distribution, Inc.Owens & Minor Distribution, Inc. is conducting a market withdrawal of MediChoice Applicator OB-GYN 8 inch product that does not meet our quality standards becau

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.