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Cleanser, Root Canal

FDA product code KJJ · Class U · Unknown

121
Registered devices
24
Adverse events
7
Recalls
41
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol
2019-06-27Inter-Med LlcThe affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prol

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