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InterActive® Healing Collar 6530-15Recalls & reported problems

Implant Direct Sybron Manufacturing LLC · Class 2 · Implant

Adverse event reports
3
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10841307109853), received between Jan 8, 2018 and Oct 28, 2021 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Failure to Osseointegrate” (2 reports).

4 other recalls cover devices cleared under the same FDA submission (K130572); 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Failure to Osseointegrate2
  • Delivered as Unsterile Product1

Patient problems

  • Failure of Implant2
  • Granuloma1
  • Insufficient Information1
  • Not Applicable1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 28, 2021Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Granuloma

    MAUDE report 12711448 ↗
  • InjuryJul 27, 2021Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Insufficient Information

    MAUDE report 12232432 ↗
  • MalfunctionJan 8, 2018Delivered as Unsterile Product; Delivered as Unsterile Product

    NO ADVERSE EVENT REPORTED. THIS LOT OF HEALING COLLARS WAS NOT STERILIZED.

    Patient problems: Not Applicable

    MAUDE report 7173976 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K130572. One submission often covers many models, so check the product and lot details in each record.

  • Z-0363-2020 · Oct 26, 2018 · Terminated
    Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX only, Sterile R Dental Implant
  • Z-1917-2018 · Mar 14, 2018 · Terminated
    ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect label on the cap says 4.3mmD Platform 604313U 13mmL. Produ
  • Z-0539-2018 · Jan 23, 2018 · Terminated
    Implant Direct, INTERACTIVE HEALING COLLAR, PART NUMBER 6530-15, 5.0mmL: 3.0mmD Platform
  • Z-2551-2018 · Mar 3, 2017 · Terminated
    ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit restorations and terminal or intermedia

Other Abutment, Implant, Dental, Endosseous devices

All Abutment, Implant, Dental, Endosseous devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.