MAUDE Adverse Event Report: BIOTECH DENTAL REFLECT RAPID; IMPLANT

Model Number	RA5010C
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	04/30/2022
Type of Reportable Event	Malfunction
Event or Problem Description
Patient (b)(6) received implant (rflt rapid ra5010c reflect rapid fixture ø5.0mm x 10 l) on (b)(6) 2021, experienced bone loss which led to a loss of integration.This led to the implant being removed on (b)(4) 2022.X-rays were not provided by the dentis.Implant replacement was sent to dr.(b)(6) on (b)(6) 2022.

• Brand Name: REFLECT RAPID
• Common Device Name: IMPLANT
• Manufacturer (Section D): BIOTECH DENTAL; 145 cedar lane; suite 205; englewood NJ 07631
• Manufacturer (Section G): BIOTECH DENTAL; 145 cedar lane; suite 205; englewood NJ 07631
• Manufacturer Contact: chris castellano ; 145 cedar lane; suite 205; englewood, NJ 07631 ; 8662775662
• MDR Report Key: 15791627
• Report Number: 3010730876-2022-00090
• Device Sequence Number: 17546777
• Product Code: DZE
• UDI-Device Identifier: 00817773024122
• UDI-Public: 00817773024122
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: K180924
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Dentist
• Remedial Action: Notification
• Type of Report: Initial
• Report Date (Section B): 11/03/2022

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: RA5010C
• Device Catalogue Number: RA5010C
• Device Lot Number: 032
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/16/2022
• Initial Report FDA Received Date: 11/14/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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
• Patient Age: 72 YR
• Patient Sex: Male