BioHorizons TLR5815Recalls & reported problems
Biohorizons Implant Systems, Inc · Tapered Internal Implant RBT, Laser-Lok 5.8 x 15mm, 5.7 Platform · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
Quick summary
This BioHorizons dental implant is a root-form implant placed in the jaw to support dental work. The 24 reports mostly describe implants that did not fuse with the surrounding bone, with no deaths and 24 injuries mentioned. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 24
- Deaths reported
- 0
- Injuries reported
- 24
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 00847236009984), received between Feb 24, 2024 and Jul 2, 2026 — classified as 24 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (23 reports).
2 other recalls cover devices cleared under the same FDA submission (K071638, K223697); 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.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate23
- Use of Device Problem1
Patient problems
- Insufficient Information24
Recent adverse event reports
The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.
InjuryJul 2, 2026Failure to Osseointegrate
InjuryMay 20, 2026Failure to Osseointegrate
InjuryMar 22, 2026Failure to Osseointegrate
InjuryFeb 18, 2026Failure to Osseointegrate
InjuryFeb 18, 2026Failure to Osseointegrate
InjuryJan 15, 2026Failure to Osseointegrate
InjuryNov 6, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 9, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 4, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 4, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJun 4, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 21, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 3, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 20358386 ↗InjuryMay 11, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 9, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 22, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 24, 2024Failure to Osseointegrate; Failure to Osseointegrate
Recalls under the same FDA submission
These recalls involve devices cleared under K071638, K223697. One submission often covers many models, so check the product and lot details in each record.
- Z-1111-2025 · Dec 6, 2024 · Open, ClassifiedTemporary Titanium Abutments
- Z-1605-2015 · Apr 16, 2015 · TerminatedTapered HD Upgrade Set, REF TSKHDUS, Non-Sterile, Rx Only, Product Usage Usage: Surgical instruments used in preparation for dental implant placement
Other Implant, Endosseous, Root-Form devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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