Data / Medical devices / Device, Thermal Ablation, Endometrial / United States
FDA-registered makers of Device, Thermal Ablation, Endometrial in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Device, Thermal Ablation, Endometrial (product code MNB). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Device, Thermal Ablation, Endometrial
- Product code
- MNB
- Country
- United States
Makers of Device, Thermal Ablation, Endometrial in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Axora Medical, Inc. | Sunnyvale, CA, United States | Complaint file establishment, Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Minerva Surgical, Inc. | Santa Clara, CA, United States | Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Channel Medsystems | Berkeley, CA, United States | Manufacturer | 0 | 1 | 2 | 0 | api.fda.gov | |
| Hologic, Inc. | Marlborough, MA, United States | Complaint file establishment, Specification developer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Hologic, Inc. | Marlborough, MA, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Microcube, LLC | Fremont, CA, United States | Manufacturer, Manufacturer for export | 0 | 1 | 0 | 0 | api.fda.gov | |
| Apical Instruments | Redwood City, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Science Outsourcing, Inc. | Brea, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, INC | Stoughton, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scientific Molding Corporation, Ltd. Dba SMC Ltd. | Santa Rosa, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vonco Products, LLC | Fortville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.