| Brand Name | MENTOR MemoryGel Breast Implant |
| Common Device Name | Prosthesis, breast, noninflatable, internal, silicone gel-filled |
| Manufacturer (Section D) |
| Mentor Texas |
| 3041 skyway circle north |
| irving TX 75038 |
|
| Manufacturer (Section G) |
| Mentor Texas |
| 3041 skyway circle north |
|
| irving TX 75038 |
|
| Manufacturer Contact |
|
henry
boden
|
| 3041 skyway circle north |
| irving, TX 75038
|
|
+1(949)788-2078
|
|
| MDR Report Key | 50952391 |
| Report Number | 1645337-2026-10900 |
| Device Sequence Number | 9624184 |
| Product Code |
FTR
|
| UDI-Device Identifier | 00081317000464 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | US |
| PMA/510(K) Number | P030053 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2022 |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional |
| 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 Expiration Date | 09/25/2026 |
| Device Catalogue Number | 3503004BC |
| Device Lot Number | 9635964 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
No
|
| Initial Date Received by Manufacturer | 09/17/2026 |
| Initial Report FDA Received Date | 09/30/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 09/28/2021 |
| 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 |
Other;
|
| Patient Age | 55 YR |
| Patient Sex | Female |
| Patient Race | White |
|
|