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FDA 510(k)

Wearable Breast Pump (Model W12)

K-Number: K252420 · 2026-02-13

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

Device Summary

Wearable Breast Pump (Model W12) is a medical device manufactured by Shenzhen TPH Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-13 under approval number K252420. 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 W12)?

Wearable Breast Pump (Model W12) 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 K252420.

When was Wearable Breast Pump (Model W12) approved by the FDA?

Wearable Breast Pump (Model W12) received FDA 510(k) clearance on 2026-02-13, under approval number K252420.

What company makes Wearable Breast Pump (Model W12)?

Wearable Breast Pump (Model W12) is manufactured by Shenzhen TPH Technology Co., Ltd..

What is the FDA product code for Wearable Breast Pump (Model W12)?

The FDA product code for Wearable Breast Pump (Model W12) 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.