MRD
- Product code
- MRD
- Device name
- Mammary Sizer
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 2 (direct download)
- 510(k) clearances (all years, FDA)
- 13 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K243271 | 2025-01-13 | Mentor Worldwide, LLC | MENTOR MemoryShape Resterilizable Gel Breast Impla… | |
| K241552 | 2024-09-06 | Mentor Worldwide, LLC | MENTOR MemoryGel Enhance Single Use Gel Sizer |
Official FDA classification page: MRD
Classification and pathway per current FDA publications. Data from openFDA (CC0).