D-PUB Electronic & Technology Co. Ltd

FDA Device Registration & Listing · Huizhou Guangdong, CN · Registration 3016159407

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016159407
FEI Number
3016159407
Entity Name
D-PUB Electronic & Technology Co. Ltd
City/State/Country
Huizhou Guangdong, CN
Establishment Address
11th Floor, Building 3, Zhongnuo Smart Valley, , Huanghou Village, Zhenlong Town, Huiyang District, Huizhou Guangdong 516227, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
JM SUNFLOWER LIMITED (Owner Number: 10047762)
Owner / Operator Contact Address
Room 109-110, 1/F., Stag Building, 148-150 Queens Road Central, Central, HK-NOTA 85200, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

New Wellness Concept SL VeDO Hummer VeDO Overdrive Plus VeDO Roco VeDO Roq VeDO Pump VeDO Hummer 2 VeDO Drive VeDO Grip VeDO Sexy Bunny VeDO Frisky Bunny VeDO Thunder Bunny VeDO Rockie VeDO Izzy

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PIA Vibrator For Climax Control Of Premature Ejaculation Gastroenterology, Urology Class 2 876.5025 2022-01-18
LKY Device, External Penile Rigidity Gastroenterology, Urology Class 2 876.5020 2014-10-29
KXQ Vibrator For Therapeutic Use, Genital Obstetrics/Gynecology Class 2 884.5960 2020-04-08

Official Correspondent

Jiri Holoubek

US Agent Details

Daniel Bilodeaux Business: Savvy Co Email: daniel@savvycompany.com Phone: (818) 2174377

Related Public Records

Same Entity

JM SUNFLOWER LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016159407. Last updated year: 2026. Please use registration number 3016159407 when referencing this establishment in official correspondence.
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