MAUDE Adverse Event Report: BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS CONICAL MULTI-UNIT STRAIGHT ABUTMENT; CONICAL MULTI-UNIT ABUTMENT

Model Number	CRMUS2N
Medical Device Problem Code	Compatibility Problem (2960)
Health Effect - Clinical Code	Insufficient Information (4580)
Type of Reportable Event	Malfunction
Event or Problem Description
This report indicates one (1) malfunction events.A review of the event involved of the device(s) experienced an connection issue.No patient adverse event was reported.No information regarding patient demographics were provided.

• Brand Name: BIOHORIZONS CONICAL MULTI-UNIT STRAIGHT ABUTMENT
• Common Device Name: CONICAL MULTI-UNIT ABUTMENT
• Manufacturer (Section D): BIOHORIZONS IMPLANT SYSTEMS; 2300 riverchase center; birmingham AL 35244
• Manufacturer (Section G): BIOHORIZONS IMPLANT SYSTEMS; 2300 riverchase center; birmingham AL 35244
• MDR Report Key: 21937168
• Report Number: 1060818-2025-70003
• Device Sequence Number: 5404711
• Product Code: NHA
• UDI-Device Identifier: 00847236025311
• UDI-Public: 00847236025311
• Combination Product (Y/N): N
• PMA/510(K) Number: K240187
• Number of Events Summarized: 1
• Summary Report (Y/N): Y
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 04/30/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: CRMUS2N
• Device Catalogue Number: CRMUS2N
• Type of Report(Section G): Periodic
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 04/30/2025
• 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
• Patient Sex: Unknown