PMA · Approved
ApprovedMinerva Endometrial Ablation System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Axora Medical, Inc. · MNB Device, Thermal Ablation, Endometrial
Approved on Feb 12, 2026 through premarket approval, which rests on the device’s own clinical evidence after a 17-day review.
- Decided
- Feb 12, 2026
- Review
- 17 days
- Class
- Class III
- Product code
- MNB
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in MNB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
Does it have a predicate?
PMA decisions do not claim a predicate device.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
How does its category compare?
All MNB devicesMNB Device, Thermal Ablation, Endometrial: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.
FDA decisions per year · MNB
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MNB
Too few MNB 510(k)s in any year since 2007 to give a median.
Recalls per year · MNB
2in 2009
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MNB
250in 2025
MAUDE reports naming product code MNB, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 9 | — | 5 | 180 |
| 2008 | 14 | — | 0 | 290 |
| 2009 | 13 | — | 2 | 792 |
| 2010 | 18 | — | 0 | 389 |
| 2011 | 18 | — | 0 | 433 |
| 2012 | 8 | — | 0 | 408 |
| 2013 | 17 | — | 0 | 368 |
| 2014 | 20 | — | 0 | 309 |
| 2015 | 7 | — | 0 | 318 |
| 2016 | 5 | — | 0 | 296 |
| 2017 | 8 | — | 0 | 292 |
| 2018 | 9 | — | 0 | 262 |
| 2019 | 8 | — | 0 | 249 |
| 2020 | 19 | — | 0 | 197 |
| 2021 | 22 | — | 0 | 229 |
| 2022 | 9 | — | 0 | 179 |
| 2023 | 16 | — | 0 | 213 |
| 2024 | 13 | — | 0 | 213 |
| 2025 | 4 | — | 0 | 250 |
| 2026 | 4 | — | 0 | — |
https://510kreport.com/device/P140013/S018 · printed Nov 5, 2026
Cite this page
510(k) Report. “P140013/S018: Minerva Endometrial Ablation System.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/P140013/S018
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026