Straumann® BLC and TLC Implants SLA Roxolid BL (REF 035.8714S)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630031764522), received between Sep 10, 2026 and Sep 10, 2026 — classified as 2 injuries.

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

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjurySep 10, 2026Difficult to Insert

  Patient problems: Fibrosis

  MAUDE report 50719474 ↗
• InjurySep 10, 2026Difficult to Insert

  The clinician reports that the day the implant was placed in ADA 6, failure occurred upon insertion. Details of surgery: Primary stability not achieved and Implant surface not completely covered with bone. Patient presented with inadequate bone quality/quantity. The device was forwarded to the manufacturer. At the event the patient experienced: Mobility. No further patient complications were reported.

  Patient problems: Fibrosis

  MAUDE report 50718741 ↗