Momcozy Wearable Breast Pump (S9 Pro, S9 Pro-A, S9 Pro-B, S9 Pro-C, S9 Pro-D, S9 ProY-A, S9 ProY-B, S9 ProY-C, S12 Pro, S12 Pro-A, S12 Pro-B, S12 Pro-C, S12 Pro-D, S12 ProY-A, S12 ProY-B, S12 ProY-C)— 510(k) K253946

Substantially Equivalent

Shenzhen Root Innovation Technology Co., Ltd.

FDA 510(k) clearance K253946 for Momcozy Wearable Breast Pump (S9 Pro, S9 Pro-A, S9 Pro-B, S9 Pro-C, S9 Pro-D, S9 ProY-A, S9 ProY-B, S9 ProY-C, S12 Pro, S12 Pro-A, S12 Pro-B, S12 Pro-C, S12 Pro-D, S12 ProY-A, S12 ProY-B, S12 ProY-C), Substantially Equivalent on 2026-04-07. Applicant: Shenzhen Root Innovation Technology Co., Ltd.. Device class: 2.

Summary

Shenzhen Root Innovation Technology's Momcozy Wearable Breast Pump is filed under product code HGX (Pump, Breast, Powered). The name lists 16 S9 and S12 model designations, and the record doesn't say how they differ.

Class II, 21 CFR 884.5160. It came in as a Traditional 510(k), and Obstetrics/Gynecology is both the classification panel and the review panel.

Shenzhen Root Innovation Technology filed from Shenzhen, China. Review took 118 calendar days (December 10, 2025 to April 7, 2026).

Clearance details

Applicant
Shenzhen Root Innovation Technology Co., Ltd.
Product code
Product code HGX
Device class
Class 2
Regulation
21 CFR 884.5160
Advisory panel
Obstetrics/Gynecology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

Recent devices under product code HGX

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Adverse events under product code HGX

product code HGX
Injury
758
Other
2
Total
760

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.