Phenox Limited

Phenox Limited holds 4 FDA 510(k) medical device clearances, first cleared 2019, most recent 2025.

Top product codes for Phenox Limited

POL — Neurology3 devices
DQX — Cardiovascular1 device

Recent clearances by Phenox Limited

K242676 — pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy DeviceCode POL·2025-02-28
K231539 — pRESET LITE Thrombectomy DeviceCode POL·2023-10-21
K222848 — pRESET Thrombectomy DeviceCode POL·2023-01-20
K191687 — pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension WireCode DQX·2019-10-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.