DiscreetDuo™ Flow Wearable Breast Pump (Model S3)
K-Number: K260259 · 2026-07-24
Device Summary
Frequently Asked Questions
What is the DiscreetDuo™ Flow Wearable Breast Pump (Model S3)?
DiscreetDuo™ Flow Wearable Breast Pump (Model S3) is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is Shenzhen TPH Technology Co., Ltd.. The 510(k) number is K260259.
When did DiscreetDuo™ Flow Wearable Breast Pump (Model S3) receive FDA 510(k) clearance?
DiscreetDuo™ Flow Wearable Breast Pump (Model S3) received FDA 510(k) clearance on 2026-07-24, under 510(k) number K260259.
Who is the listed applicant for DiscreetDuo™ Flow Wearable Breast Pump (Model S3)?
The FDA 510(k) record lists Shenzhen TPH Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DiscreetDuo™ Flow Wearable Breast Pump (Model S3)?
The FDA product code for DiscreetDuo™ Flow Wearable Breast Pump (Model S3) is HGX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Shenzhen TPH Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HGX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.