| Brand Name | EMPHASYS |
| Common Device Name | Hip Implant : Acetabular Cup |
| Manufacturer (Section D) |
| DePuy Ireland - 3015516266 |
| loughbeg ringaskiddy co. |
| cork |
| EI |
|
| Manufacturer (Section G) |
| Cork Mfg & Material Warehouse |
| loughbeg ringaskiddy |
|
| cork |
|
EI
|
|
| Manufacturer Contact |
|
elba
bello
|
| 700 orthpaedic dr. |
| warsaw, IN 46581
|
|
+1(908)386-3534
|
|
| MDR Report Key | 50575601 |
| Report Number | 1818910-2026-15092 |
| Device Sequence Number | 13311071 |
| Product Code |
LPH
|
| UDI-Device Identifier | 10603295500612 |
| Combination Product (Y/N) | N |
| Initial Reporter State | PA |
| Initial Reporter Country | US |
| PMA/510(K) Number | K231873 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Device Implanted Year | 2026 |
| Device Explanted Year | 2026 |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional,Company Representative |
| Initial Reporter Occupation |
Physician
|
| 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 | 471054300 |
| Device Lot Number | 4998581 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Initial Date Received by Manufacturer | 08/10/2026 |
| Initial Report FDA Received Date | 09/02/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 11/24/2025 |
| 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 | 70 YR |
| Patient Sex | Male |
| Patient Weight | 210 LB |