FDA 510(k)

Mother's Nature W1 Warming Wearable Breast Pump

N.º K: K260864 · 2026-06-09

SolicitanteShenzhen TPH Technology Co., Ltd.

Fecha de decisión2026-06-09

Código de productoHGX

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

Mother's Nature W1 Warming Wearable Breast Pump is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen TPH Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-06-09 under 510(k) number K260864. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Mother's Nature W1 Warming Wearable Breast Pump?

Mother's Nature W1 Warming Wearable Breast Pump is a medical device that received FDA 510(k) clearance on 2026-06-09. The listed applicant is Shenzhen TPH Technology Co., Ltd.. The 510(k) number is K260864.

When did Mother's Nature W1 Warming Wearable Breast Pump receive FDA 510(k) clearance?

Mother's Nature W1 Warming Wearable Breast Pump received FDA 510(k) clearance on 2026-06-09, under 510(k) number K260864.

Who is the listed applicant for Mother's Nature W1 Warming Wearable Breast Pump?

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 Mother's Nature W1 Warming Wearable Breast Pump?

The FDA product code for Mother's Nature W1 Warming Wearable Breast Pump is HGX.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Otros registros que enlistan a Shenzhen TPH Technology Co., Ltd. como solicitante

K254203Wearable Breast Pump (Model S36)K260259DiscreetDuo™ Flow Wearable Breast Pump (Model S3)K261199Wearable Breast Pump (Model S32A)K254244Wearable Breast Pump (Model S39)K260033Wearable Breast Pump (Model S21A)K252422Wearable Breast Pump (Model W2)

Ver todos los 24 dispositivos →

Dispositivos relacionados (Código: HGX)

K254203Wearable Breast Pump (Model S36)Shenzhen TPH Technology Co., Ltd.K261622Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62)Philips Consumer Lifestyle B.V.K262774Wearable breast pump (Model: XN/MD-2249BS, ZFHF)Guangdong Horigen Mother & Baby Products Co., Ltd.K260643Cimilre Dual MaxCimilre Co., Ltd.K261298Wearable Electric Breast Pump (YM-8837, YM-8838, YM-8856(H03), YM-8809(S42))Guangdong Youmeng Electrical Technology Co., Ltd.K260259DiscreetDuo™ Flow Wearable Breast Pump (Model S3)Shenzhen TPH Technology Co., Ltd.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.