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Aligner, Bracket, Orthodontic

FDA product code ECQ · Class 1 · Dental

67
Registered devices
5
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-11-13Karl Storz Endoscopy America IncKARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material use

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