MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,literature report with the FDA on 2017-02-20 for ENDOBON GRANULES N/A manufactured by Biomet France S.a.r.l..
[67804876]
The product identification necessary to review manufacturing history was not provided. Current information is insufficient to permit a conclusion as to the cause of the event. The following sections could not be completed with the limited information provided. Date of event - ni expiration date? Ni date implanted - ni manufacture date? Ni concomitant medical product(s): - unknown dental implant. Therapy date - ni. Barone et al. "a prospective, randomized, controlled, multicenter evaluation of extraction socket preservation comparing two bovine xenografts: clinical and histologic outcomes" the international journal of periodontics & restorative dentistry. Volume 33, number 6, 2014. 795-803. - attachment: [barone et al. Pdf]
Patient Sequence No: 1, Text Type: N, H10
[67804877]
It was reported in a journal article one patient's dental implant did not successfully integrate.
Patient Sequence No: 1, Text Type: D, B5
[79315102]
Upon receipt of additional information, this product was determined to not be reportable. The product involved in the event was not manufactured by zimmer biomet; rather, a competitor product was implanted at the time of the failure. The initial report was submitted in error and should be voided.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3006946279-2017-00044 |
| MDR Report Key | 6344053 |
| Report Source | FOREIGN,LITERATURE |
| Date Received | 2017-02-20 |
| Date of Report | 2017-06-26 |
| Date Mfgr Received | 2017-06-25 |
| Date Added to Maude | 2017-02-20 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. CHRISTINA ARNT |
| Manufacturer Street | 56 E. BELL DR. |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal | 46582 |
| Manufacturer Phone | 5745273773 |
| Manufacturer G1 | BIOMET FRANCE S.A.R.L. |
| Manufacturer Street | PLATEAU DE LAUTAGNE BP75 |
| Manufacturer City | VALENCE CEDEX 26903 |
| Manufacturer Country | FR |
| Manufacturer Postal Code | 26903 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | N/A |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ENDOBON GRANULES |
| Generic Name | BONE GRAFTING MATERIAL, SYNTHETIC |
| Product Code | LYC |
| Date Received | 2017-02-20 |
| Model Number | N/A |
| Catalog Number | NI |
| Lot Number | NI |
| ID Number | N/A |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BIOMET FRANCE S.A.R.L. |
| Manufacturer Address | PLATEAU DE LAUTAGNE BP75 VALENCE CEDEX 26903 FR 26903 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-02-20 |