MAUDE Adverse Event Report: IMPLANT DIRECT SYBRON MANUFACT LEGACY2 SBM IMPLANT 5.2DX11L 4.5MMD PLAT; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	825211
Medical Device Problem Codes	Separation Failure (2547); Insufficient Device Problem Information (3190)
Health Effect - Clinical Codes	Inadequate Osseointegration (2646); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/13/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Reviewed attached customer feedback form: (b)(4) contraindications relevant to failure: component does not disengage.Part number: 825211 revision: c visual: contaminated condition.Received 825211 assy.In an opened vial.It was difficult to break the fixation screw loose.Once the screw was broken loose and the assembly was taken apart, a thin film of dried blood / saliva could be seen inside the bore of the transfer.Dried blood acts as a glue or sealant thus potentially locking the screw in place.The assembly was reassembled and disassembled multiple times with no trouble or effort.See photos.Complaint is not confirmed.Specification should be: length:.463 specification as found:.463 diameter:.2021/.2036 specification as found:.2026 comments: rbs (b)(6) 2025.
Event or Problem Description
Component does not disengage.

• Brand Name: LEGACY2 SBM IMPLANT 5.2DX11L 4.5MMD PLAT
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): IMPLANT DIRECT SYBRON MANUFACT; 3050 east hillcrest drive; thousand oaks CA 91362
• Manufacturer (Section G): IMPLANT DIRECT SYBRON MANUFACT; 3050 east hillcrest drive; thousand oaks CA 91362
• Manufacturer Contact: anitha mechery ; 3050 east hillcrest drive; thousand oaks 91362 ; 8057785975
• MDR Report Key: 23533738
• Report Number: 3001617766-2025-008935
• Device Sequence Number: 9084006
• Product Code: DZE
• UDI-Device Identifier: 10841307101444
• UDI-Public: (01)10841307101444(10)15025410(17)300326
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K192221
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Remedial Action: Replace
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: 825211
• Device Lot Number: 15025410
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 11/12/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/27/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 53 YR
• Patient Sex: Male
• Patient Weight: 189 KG