FDA Device Intelligence
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Controller, Foot, Handpiece And Cord

FDA product code EBW · Class 1 · Dental

523
Registered devices
392
Adverse events
2
Recalls
61
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-12-21W & H DentalWerk Burmoos GMBH - Site 1During continuous postmarket surveillance activities, we have noticed a potential malfunction of individual foot controls of the type S-N1/S-N2. In case the err
2013-10-24Nobel Biocare Usa LlcThe recall was initiated because there is a potential for malfunction of the OsseoCare Pro when used with the OseeoCare Pro iPad application software release 1.

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