510(k) K260259

DiscreetDuo™ Flow Wearable Breast Pump (Model S3) by Shenzhen TPH Technology Co., Ltd. — Product Code HGX

K260259 is an FDA 510(k) premarket notification submitted by Shenzhen TPH Technology Co., Ltd. for the device "DiscreetDuo™ Flow Wearable Breast Pump (Model S3)". The FDA issued a decision of Substantially Equivalent on July 24, 2026. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Shenzhen TPH Technology Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 2026
Date Received
January 28, 2026
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Breast, Powered
Device Class
Class II
Regulation Number
884.5160
Review Panel
OB
Submission Type