Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012062596

FEI Number

3012062596

Entity Name

Solstice Electronic Technologies ( Dongguan) Limited

City/State/Country

Dongguan City Guangdong, CN

Establishment Address

2/F, No.138-102 , Tianzhai Group, Yisha Village , Shatian Town, Dongguan City Guangdong 00000, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Solstice Technologies Limited (Owner Number: 10048812)

Owner / Operator Contact Address

Rooms 2305-07 Wayson Commercial Building, 28 Connaught road West, Sheung Wan, HK-NOTA 00000, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Evenflo Advanced Double Electric Pump EVENFLO POCKET PORTABLE DOUBLE ELECTRIC BREAST PUMP Evenflo Electric Breast Pump Evenflo Manual Breast Pump

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGX	Pump, Breast, Powered	Obstetrics/Gynecology	Class 2	884.5160	2015-03-05
HGX	Pump, Breast, Powered	Obstetrics/Gynecology	Class 2	884.5160	2026-01-07
HGX	Pump, Breast, Powered	Obstetrics/Gynecology	Class 2	884.5160	2015-03-05
HGY	Pump, Breast, Non-Powered	Obstetrics/Gynecology	Class 1	884.5150	2015-03-05

Official Correspondent

Hughes Sanoner

US Agent Details

Michael Dressman Business: Evenflo Feeding Inc Email: Michael.Dressman@kcc.com Phone: (937) 8303646

Related Public Records

Same Entity

Solstice Technologies Limited

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K190465	Hygeia II Medical Group, Inc.	Evolve Breast Pump	2019-10-18
K021739	Limerick, Inc.	LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002	2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012062596. Last updated year: 2026. Please use registration number 3012062596 when referencing this establishment in official correspondence.