FDA 510(k) clearances
- K160221 Β· Implance Dental Implant System, Implance Dental Abutment System Β· 2016-09-12
A 510(k) clearance means the FDA found the device substantially equivalent to one already legally sold. It is not a quality ranking.
Recalls
We have not yet searched the recall databases system by system for Implance.
No result is not proof that no recall or field safety notice exists in any country.
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Educational information only. Choosing an implant requires an examination by a qualified dentist. Implance are trademarks of Implance. DentalImplantBrands is not affiliated with or endorsed by Implance.
