Skip to content

Prima Implant System 15636KRecalls & reported problems

Keystone Dental, Inc. · Implant · Class 2 · Implant

All models of Prima Implant System (58)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
20
Deaths reported
0
Injuries reported
20
Recalls naming it
0

Summary

The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI D76815636K0), received between Feb 3, 2020 and Dec 8, 2025 — classified as 20 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (16 reports).

7 other recalls cover devices cleared under the same FDA submission (K051614, K072768); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate16
  • Loss of Osseointegration4

Patient problems

  • Inadequate Osseointegration12
  • Failure of Implant4
  • Osteopenia/ Osteoporosis2
  • Implant Pain1
  • Osteolysis1
  • Pain1

Recent adverse event reports

The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 8, 2025Loss of Osseointegration; Loss of Osseointegration

    LOSS OF OSSEOINTEGRATION.

    Patient problems: Inadequate Osseointegration

    MAUDE report 23738564 ↗
  • InjurySep 3, 2025Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 22952716 ↗
  • InjuryMar 18, 2024Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 18922667 ↗
  • InjuryJun 27, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Implant Pain; Inadequate Osseointegration

    MAUDE report 17210882 ↗
  • InjuryJun 22, 2023Loss of Osseointegration; Loss of Osseointegration

    LOSS OF OSSEOINTEGRATION.

    Patient problems: Inadequate Osseointegration

    MAUDE report 17181269 ↗
  • InjuryJun 16, 2023Loss of Osseointegration; Loss of Osseointegration

    LOSS OF OSSEOINTEGRATION.

    Patient problems: Inadequate Osseointegration

    MAUDE report 17142863 ↗
  • InjuryJun 15, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 17139460 ↗
  • InjuryJun 15, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 17138702 ↗
  • InjuryJun 6, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE

    Patient problems: Inadequate Osseointegration

    MAUDE report 17075277 ↗
  • InjuryMay 12, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 16918857 ↗
  • InjuryJan 18, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 16196568 ↗
  • InjuryJan 18, 2023Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Inadequate Osseointegration

    MAUDE report 16195140 ↗
  • InjuryJul 20, 2022Loss of Osseointegration; Loss of Osseointegration

    LOSS OF OSSEOINTEGRATION.

    Patient problems: Osteolysis

    MAUDE report 15070078 ↗
  • InjuryApr 13, 2022Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 14106989 ↗
  • InjuryOct 25, 2021Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 12694090 ↗
  • InjuryJul 19, 2021Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 12187803 ↗
  • InjuryApr 21, 2021Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Osteopenia/ Osteoporosis

    MAUDE report 11704053 ↗
  • InjuryMar 18, 2021Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Pain

    MAUDE report 11521037 ↗
  • InjuryDec 17, 2020Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Osteopenia/ Osteoporosis

    MAUDE report 11033484 ↗
  • InjuryFeb 3, 2020Failure to Osseointegrate; Failure to Osseointegrate

    FAILURE TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 9661822 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051614, K072768. One submission often covers many models, so check the product and lot details in each record.

  • Z-2162-2018 · May 1, 2018 · Terminated
    Prima Plus 4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single
  • Z-1179-2018 · Oct 16, 2017 · Terminated
    STAGE-1 RDS COC Abutment Plastic Sleeve, Non-Lock, Multi-Unit; Catalog Number: S2437-01-1K
  • Z-0727-2018 · Aug 25, 2017 · Terminated
    Stage-1 RDS Indexed Abutment for RDS Stage-1 Single Stage Implants Keystone s implants are intended for use in partially or fully edentulous mandibles and maxillae, in support
  • Z-0608-2018 · Jun 20, 2017 · Terminated
    Multi-Unit Abutment Angled, 17, 4mm Cuff 4.1/4.5mm TiLobe Implants, Catalog Number 45324K pRODUCT Usage: Use in partially or fully edentulous mandibles and maxillae, in support of
  • Z-1818-2017 · Mar 9, 2017 · Terminated
    Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K
  • Z-0299-2017 · Sep 15, 2016 · Terminated
    Keystone Dental PrimaConnex Straight Implant TC, RD Internal Connection 4.0 x 11.5mm. Product code:15613K Implants are intended for use in partially or fully edentulous mandibles a
  • Z-0973-2013 · Mar 11, 2013 · Terminated
    PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

All IMPLANT, ENDOSSEOUS, ROOT-FORM devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page