NANNING VV DENTAL CO., LTD.

FDA Device Registration & Listing · Nanning Guangxi, CN · Registration 3014315145

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
3014315145
FEI Number
3014315145
Entity Name
NANNING VV DENTAL CO., LTD.
City/State/Country
Nanning Guangxi, CN
Establishment Address
No. 501, 5th Floor and No. 601, 6th Floor, No. 1 Preparation Workshop, Jinhong Pharmaceutical Production Base,, No. 7 Luolai Road, Xixiangtang District, Nanning City, Guangxi 530007 China, Nanning Guangxi 530007, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NANNING VV DENTAL CO., LTD. (Owner Number: 10056843)
Owner / Operator Contact Address
No. 501, 5th Floor and No. 601, 6th Floor, No. 1 Preparation Workshop, Jinhong Pharmaceutical Production Base,, No. 7 Luolai Road, Xixiangtang District, Nanning City,Guangxi 530007 China, Nanning, CN-GX 530007, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Scaler,ultrasonic VET-1,VET-W3,VET-W3-LED,VET-6,WET-6-LED,VET-W7,WET-W7-LED,VST-1,VST-W3,VST-6,VST-W7 Scaler,ultrasonic E2,P2,SK-E1,SK-D1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ELC Scaler, Ultrasonic Dental Class 2 872.4850 2018-01-22

Official Correspondent

Chaojun Liang

US Agent Details

CHEN JINGYUAN Business: SEA 2 SKY STORE LLC Email: jasminetamura@gmail.com Phone: (503) 9263661

Related Public Records

Same Entity

NANNING VV DENTAL CO., LTD.
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
K832443 California Technics, Inc. ULTRASONIC DENTAL PROPHYLAXIS UNIT 1983-09-12
K994299 Bonart Co., Ltd. ART-P3, MODEL P3-1-ART-A1 2000-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014315145. Last updated year: 2026. Please use registration number 3014315145 when referencing this establishment in official correspondence.
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