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MIS implant clearances and recalls: the public record

The FDA database lists 14 endosseous implant 510(k) clearances for MIS, the first in 2001. Below are selected recent ones.

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FDA 510(k) clearances

  • K251647 · MIS C1, MIS Seven, MIS M4, MIS Lance implant systems · 2025-08-21
  • K251297 · MIS LYNX Conical Connection Implant System · 2025-07-24
  • K180282 · MIS Internal Hex Dental Implant System · 2018-06-22
  • K172505 · MIS C1 Narrow Platform Conical Connection Implant System · 2017-12-28
  • K163349 · MIS V3 Conical Connection Dental Implant System · 2017-05-26
  • K003191 · MIS Implant System · 2001-09-28

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 MIS.

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

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