ACULA TECHNOLOGY CORP

FDA Device Registration & Listing · Luchu Taoyuan, TW · Registration 3003032840

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
3003032840
FEI Number
3003032840
Entity Name
ACULA TECHNOLOGY CORP
City/State/Country
Luchu Taoyuan, TW
Establishment Address
11, Alley 21, Lane 20, Dashing Rd.,, Luchu Dist., Taoyuan City, Taiwan, Luchu Taoyuan 33862, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ACULA TECHNOLOGY CORP. (Owner Number: 10032010)
Owner / Operator Contact Address
11, Alley 21, Lane 20, Dashing Rd.,, Luchu Dist., Taoyuan City, Taiwan, Luchu, TW-TAO 33862, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

LUMIN UMD5-21B01 ME2-24B23 ME1-19A01 ME2-24A01 LUMIN UMD3-21B01

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HJG System, Reading, Television, Closed-Circuit Ophthalmic Class 1 886.5820 2010-03-30
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2024-10-24
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2026-04-16
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2024-10-24

Official Correspondent

No official correspondent registered.

US Agent Details

Aries Chu Email: arieschu@gmail.com Phone: (341) 4009102

Related Public Records

Same Entity

ACULA TECHNOLOGY CORP.
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
K920069 Innoventions, Inc. MAGNI-CAM 1992-03-02
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 3003032840. Last updated year: 2026. Please use registration number 3003032840 when referencing this establishment in official correspondence.
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