Anker Innovations Limited

Anker Innovations Limited holds 2 FDA 510(k) medical device clearances, first cleared 2025, most recent 2026.

Top product codes for Anker Innovations Limited

HGX — Obstetrics/Gynecology2 devices

Recent clearances by Anker Innovations Limited

K254300 — eufy Wearable Breast Pump (T600P, T6000, T6001, T6002, T6003, T6004, T6005, T6006, T6007, T6008, T6009)Code HGX·2026-05-29
K250207 — eufy Wearable Breast Pump S1 (T8D02); eufy Wearable Breast Pump E10 (T8D03)Code HGX·2025-08-11

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