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FDA 510(k)

Wearable Breast Pump (Model W2)

K-Number: K252422 · 2026-02-13

Decision Date2026-02-13
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Wearable Breast Pump (Model W2) is a medical device manufactured by Shenzhen TPH Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-13 under approval number K252422. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wearable Breast Pump (Model W2)?

Wearable Breast Pump (Model W2) is a medical device that received FDA 510(k) clearance on 2026-02-13. It is manufactured by Shenzhen TPH Technology Co., Ltd.. The 510(k) number is K252422.

When was Wearable Breast Pump (Model W2) approved by the FDA?

Wearable Breast Pump (Model W2) received FDA 510(k) clearance on 2026-02-13, under approval number K252422.

What company makes Wearable Breast Pump (Model W2)?

Wearable Breast Pump (Model W2) is manufactured by Shenzhen TPH Technology Co., Ltd..

What is the FDA product code for Wearable Breast Pump (Model W2)?

The FDA product code for Wearable Breast Pump (Model W2) is HGX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.