MNBClass III

Device, Thermal Ablation, Endometrial

Name: FDA product code MNB: Device, Thermal Ablation, Endometrial
License: https://open.fda.gov/license/

Unknown

MNB is the FDA product code for Device, Thermal Ablation, Endometrial, a class III device type. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and 12 recalls.

Classification record

Product code: MNB
Device name: Device, Thermal Ablation, Endometrial
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 12

Companies listing this code with FDA

Companies whose registered establishments list this code

Apical Instruments
Axora Medical, Inc.
Brdh
Channel Medsystems
Hologic Surgical Products Costa Rica, S.r.l.
Hologic, Inc.
Isomedix Operations Inc
Life Science Outsourcing, Inc.
Mdtglobal, A.S.
Microcube, LLC
Minerva Surgical, Inc.
Primo Medical Group, Inc

12 of 17 companies shown, in name order