DIVA LABORATORIES, LTD.

FDA Device Registration & Listing · NEW TAIPEI CITY, TAIPEI-DISTRICT, 235, TW · Registration 3007817002

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
3007817002
FEI Number
3007817002
Entity Name
DIVA LABORATORIES, LTD.
City/State/Country
NEW TAIPEI CITY, TAIPEI-DISTRICT, 235, TW
Establishment Address
9F. NO.351, SEC.2 ZHONGSHAN ROAD, ZHONGHE DIST., NEW TAIPEI CITY, TAIPEI-DISTRICT, 235 235, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DIVA Laboratories, Ltd. (Owner Number: 10050307)
Owner / Operator Contact Address
9F. No.351, Sec.2 Zhongshan Road, Zhonghe Dist., New Taipei City, TW-TPE 235, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

GUP2103CMI

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2024-12-03

Official Correspondent

Rongchi Liao

US Agent Details

Kevin Chen Business: DIVA LABORATORIES US LLC Email: kevin_chen@diva.com.tw Phone: (973) 9838809

Related Public Records

Same Entity

DIVA Laboratories, 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
K163335 Eizo Corporation 6MP Color LCD Monitor, RadiForce RX660, RX660-AR 2016-12-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007817002. Last updated year: 2026. Please use registration number 3007817002 when referencing this establishment in official correspondence.
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