Microsulis Medical, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 3
What Microsulis Medical, Ltd. makes
Microsulis Medical, Ltd. manufactures the Microsulis Microwave Endometrial Ablation (MEA) System, a device designed for endometrial ablation procedures to treat abnormal uterine bleeding.
The company’s portfolio is regulated under Class III classification in the United States, with the MEA System listed under the FDA’s Premarket Approval (PMA) pathway. The manufacturer is based in the US.
Catalogue
Acculis ACCU2I Pmta Applicator Model ACCU2I Ref K094021
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Microsulis Medical, Ltd. have in the registry?
The registry currently lists 3 devices for Microsulis Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microsulis Medical, Ltd.'s devices?
Among its 3 most recently registered devices, Microsulis Medical, Ltd. has devices listed in FDA 510(k) (2 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Microsulis Medical, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Microsulis Medical, Ltd.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Microsulis Medical, Ltd. in the registry?
The most recently registered devices listed for Microsulis Medical, Ltd. include ACCULIS ACCU2I PMTA APPLICATOR MODEL ACCU2I, ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR and MICROSULIS MICROWAVE ENDOMETERIAL ABLATION (MEA) SYSTEM.