Skip to the page

Data / Medical devices / Hong Kong / Anker Innovations Limited

Anker Innovations Limited: FDA-registered device maker in Hong Kong, Hong Kong, 3 510(k) clearances

Anker Innovations Limited is registered with the FDA (registration 3013684412) in Hong Kong, Hong Kong. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated May 29, 2026. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3013684412
Address
Unit 56, 8th Floor, Tower 2, Admiralty Centre 18 Harcourt Road, Hong Kong, Hong Kong, None
Owner or operator
Anker Innovations Limited (10055329)
Roles
Exporter to the US, Manufacturer, Repackager or relabeler, Specification developer
First device listed
September 22, 2025
Registered through
2026
Brand names listed
eufy Wearable Breast Pump E10 (T8D03), eufy Wearable Breast Pump E20 (T6060), eufy Wearable Breast Pump S1 (T8D02), eufy Wearable Breast Pump S2, eufy Wearable Breast Pump S2 Pro

Devices it lists

DeviceProduct codeClassRoleSource
Pump, Breast, PoweredHGX2Exporter to the US, Manufacturer, Repackager or relabeler, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 29, 2026K254300eufy Wearable Breast Pump (T600P, T6000, T6001, T6002, T6003, T6004, T6005, T6006, T6007, T6008, T6009)HGXSubstantially EquivalentAnker Innovations Limitedaccessdata.fda.gov
August 11, 2025K250207eufy Wearable Breast Pump S1 (T8D02); eufy Wearable Breast Pump E10 (T8D03)HGXSubstantially EquivalentAnker Innovations Limitedaccessdata.fda.gov
April 2, 2025K250152eufy Wearable Breast Pump S1 (T8D02) Model T8D02; eufy Wearable Breast Pump E10 (T8D03) Model T8D03; eufy Wearable Breast Pump S1 Pro (T8D04) Model T8D04; eufy Wearable Breast Pump E20 (T6060) Model T6060;HGXSubstantially EquivalentShenzhen TPH Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 29, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.