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Anker Innovations Limited

CN Last updated 23 Oct 2026

Devices
6
Registries
GUDIDFDA 510(k)FDA
FDA recalls
0

Catalogue6

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Anker Innovations Limited Hong Kong · HK FEI 3013684412

What Anker Innovations Limited makes

Anker Innovations Limited manufactures wearable breast pumps, including the eufy Wearable Breast Pump S1 and eufy Wearable Breast Pump E10. These devices are designed for lactating individuals to express milk discreetly and hands-free.

The company’s wearable breast pumps are classified as Class II medical devices in the US and are listed under the FDA’s 510(k) pathway. The products are registered in the FDA’s 510(k) database. Anker Innovations Limited is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Anker Innovations Limited manufacture?

Anker Innovations Limited specializes in wearable breast pumps, such as the eufy Wearable Breast Pump S1 and eufy Wearable Breast Pump E10. These devices are designed to help lactating individuals express milk discreetly and without the need for manual handling, making breastfeeding more convenient.

Where is Anker Innovations Limited based?

Anker Innovations Limited is headquartered in the United States. The company’s location is relevant for understanding its regulatory oversight and compliance with US medical device regulations.

How are Anker Innovations Limited’s wearable breast pumps classified in the US?

The wearable breast pumps manufactured by Anker Innovations Limited are classified as Class II medical devices under US regulations. This classification typically applies to devices with moderate risk, requiring special controls to ensure safety and effectiveness beyond general controls.

Are Anker Innovations Limited’s devices listed in any regulatory registries?

Yes, Anker Innovations Limited’s wearable breast pumps are registered in the FDA’s 510(k) database. This pathway is used for devices that are substantially equivalent to legally marketed predicates, demonstrating compliance with regulatory requirements before commercial distribution.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
CN
Website
eufy.com
Phone
+1 (800)994 3056
DUNS number
663903915