| Brand Name | GreenLight XPS |
| Common Device Name | Powered Laser Surgical Instrument |
| Manufacturer (Section D) |
| AMERICAN MEDICAL SYSTEMS |
| innovation ctr, silicon valley |
| 3070 orchard drive |
| san jose CA 95134 -201 |
|
| Manufacturer (Section G) |
| Boston Scientific Corporation |
| 4100 hamline avenue north |
|
| saint paul MN 55112 -579 |
|
| Manufacturer Contact |
|
farshad
fahimi
|
| 4100 hamline avenue north |
| building c |
| saint paul, MN 55112
|
|
| MDR Report Key | 50923706 |
| Report Number | 2124215-2026-51542 |
| Device Sequence Number | 14801007 |
| Product Code |
GEX
|
| UDI-Device Identifier | 00878953001906 |
| UDI-Public | (01)00878953001906(11)110601(10)XPS50354 |
| Combination Product (Y/N) | N |
| Initial Reporter State | MN |
| Initial Reporter Country | US |
| PMA/510(K) Number | K092735 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/28/2026 |
| 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 | 0010-0210R |
| Device Catalogue Number | 0010-0210R |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 09/14/2026 |
| Initial Report FDA Received Date | 09/28/2026 |
| Date Device Manufactured | 06/01/2011 |
| Is the Device Labeled for Single Use? (Y/N) |
No
|
| Usage of Device |
Reuse
|
| Patient Sequence Number | 1 |
| Patient Age | 69 YR |
| Patient Sex | Female |