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Myringotomy Procedure Kit

FDA product code OGS · Class 2 · Ear, Nose, Throat

125
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-11-17MEDLINE INDUSTRIES, LP - NorthfieldSterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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