Anker Innovations Limited

FDA Device Registration & Listing · Hong Kong, HK · Registration 3013684412

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013684412
FEI Number
3013684412
Entity Name
Anker Innovations Limited
City/State/Country
Hong Kong, HK
Establishment Address
Unit 56, 8th Floor, Tower 2, Admiralty Centre, 18 Harcourt Road, Hong Kong None, HK
Establishment Type(s)
Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Anker Innovations Limited (Owner Number: 10055329)
Owner / Operator Contact Address
Unit 56, 8th Floor, Tower 2, Admiralty Centre, 18 Harcourt Road, Hong Kong, HK-NOTA None, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Eufy: T9120, T9146, T9147, T9148, T9149, T9150 eufy Wearable Breast Pump E10 (T8D03) eufy Wearable Breast Pump S1 Pro (T8D04) eufy Wearable Breast Pump E20 (T6060) eufy Wearable Breast Pump S1 (T8D02) eufy Wearable Breast Pump E10 (T8D03) eufy Wearable Breast Pump S1 (T8D02) eufy Wearable Breast Pump S1 Pro (T8D04) eufy Wearable Breast Pump E20 (T6060)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PUH Analyzer, Body Composition, Exempt Cardiovascular Class 2 870.2770 2020-02-28
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2026-02-25
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2025-09-22

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Anker Innovations Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190465 Hygeia II Medical Group, Inc. Evolve Breast Pump 2019-10-18
K021739 Limerick, Inc. LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013684412. Last updated year: 2026. Please use registration number 3013684412 when referencing this establishment in official correspondence.
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