| Brand Name | MyoSure Tissue Removal Device |
| Common Device Name | HYSTEROSCOPE (AND ACCESSORIES) |
| Manufacturer (Section D) |
| HOLOGIC, INC |
| 250 campus drive |
| marlborough MA 01752 |
|
| Manufacturer (Section G) |
| HOLOGIC, INC |
| 250 campus drive |
|
| marlborough MA 01752 |
|
| Manufacturer Contact |
|
simran
keswani
|
| 250 campus drive |
| marlborough, MA 01752
|
|
| MDR Report Key | 50165962 |
| Report Number | 1222780-2026-00479 |
| Device Sequence Number | 5305280 |
| Product Code |
HIH
|
| UDI-Device Identifier | 15420045505070 |
| UDI-Public | 15420045505070 |
| Combination Product (Y/N) | N |
| Initial Reporter State | MI |
| Initial Reporter Country | US |
| PMA/510(K) Number | K142029 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
User Facility,Company Representative |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
08/06/2026 |
| 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 | 30-401LITE |
| Device Catalogue Number | 30-401LITE |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 07/22/2026 |
| Initial Report FDA Received Date | 08/06/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| 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 Sex | Unknown |