FDA 510(k) Applications Submitted by Pollogen Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K203665 12/16/2020 STOP U Model UXV Device Pollogen Ltd.
K182774 10/01/2018 STOP U (Packed Black USA), STOP U (Packed White USA) Pollogen Ltd.
K173503 11/13/2017 Pollogen Legend System Pollogen Ltd.
K220322 02/03/2022 Pollogen STOP U Model UXV Device Pollogen Ltd.
K171359 05/09/2017 Pollogen Legend+ System Pollogen Ltd.
K243217 10/03/2024 Legend X Desktop System Pollogen Ltd.
K233766 11/24/2023 Geneo X Elite Pollogen Ltd.
K240999 04/11/2024 Legend X Applicator VO Pollogen Ltd.
K220124 01/18/2022 YandR System, VoluDerm Handpiece, VoluDerm Tips Pollogen Ltd.


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