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Ear Wick

FDA product code KCN · Class 1 · Ear, Nose, Throat

113
Registered devices
1
Adverse events
6
Recalls
4
510(k) clearances

Devices with this code

OSSEOUS PVA Wick and Wipe — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDOTOCELL® Ear Wick — Boston Medical Products, Inc.NETCELL — NETWORK MEDICAL PRODUCTS LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDGyrus ACMI — Gyrus ACMI, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDMerocel — MEDTRONIC XOMED, INC.OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDMerocel® — MEDTRONIC XOMED, INC.OSSEOUS — EON MEDITECH PRIVATE LIMITEDFABCO — FIRST AID BANDAGE CO INCNETCELL — NETWORK MEDICAL PRODUCTS LIMITEDCollin — NETWORK MEDICAL PRODUCTS LIMITEDMerocel® — MEDTRONIC XOMED, INC.Ultracell® — Beaver-Visitec International, Inc.OSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS PVA Corneal Light Shield — EON MEDITECH PRIVATE LIMITEDMerocel® — MEDTRONIC XOMED, INC.OSSEOUS PVA Eye Drain Large — EON MEDITECH PRIVATE LIMITEDFABCO — FIRST AID BANDAGE CO INCMerocel® — MEDTRONIC XOMED, INC.NA — Summit Medical, Inc.

Recent recalls

DateFirmReason
2022-05-25Mckesson Medical-Surgical Inc. Corporate OfficeFacility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lot
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised
2003-01-08Ultracell Medical TechnologiesSterility of the device is compromised

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