Unisense Fertilitech A/S

Denmark(FDA 510(k) applicant) Last updated 22 Oct 2026

Devices: 4
Registries: FDA 510(k)
FDA recalls: 0

Catalogue4

Embryoscope Ref K111715

Class II FDA 510(k) Active
Embryoscope And Embryoslide Ref K092183

Class II FDA 510(k) Active
Embryo Viewer Software Ref K113075

Class II FDA 510(k) Active
Embryoviewer Software Ref K133712

Class II FDA 510(k) Active

Information

Country: Denmark(Country (from FDA 510(k) applicant address))