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Implant Direct implant clearances and recalls: the public record

The FDA database lists 13 endosseous implant 510(k) clearances for Implant Direct, the first in 2006. Below are selected recent ones.

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FDA 510(k) clearances

  • K222211 · Implant Direct Dental Implant Systems Portfolio - MR Conditional · 2023-02-02
  • K201553 · Simply Iconic Implants · 2021-01-22
  • K192221 · Legacy2, Legacy3, Legacy4, simplyLegacy2, simplyLegacy3 dental implants · 2020-06-25
  • K143011 · InterActive/SwishActive System · 2015-07-16
  • K073033 · Legacy Dental Implants · 2007-12-10

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 Implant Direct.

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. Implant Direct are trademarks of Implant Direct. DentalImplantBrands is not affiliated with or endorsed by Implant Direct.

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