AURORA OPTIC INC.

FDA Device Registration & Listing · CHIAYI, TW · Registration 3013202270

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
3013202270
FEI Number
3013202270
Entity Name
AURORA OPTIC INC.
City/State/Country
CHIAYI, TW
Establishment Address
no. 6 INDUSTRIAL FIFTH ROAD, TOU CHIAU, INDUSTRIAL PARK, CHIAYI 621012, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AURORA OPTIC INC. (Owner Number: 10052355)
Owner / Operator Contact Address
no. 6 INDUSTRIAL FIFTH ROAD, TOU CHIAU, INDUSTRIAL PARK, CHIAYI, TW-CYQ 62155, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Magnifier, Hand-Held, Low-Vision Lens, spectacle (prescription), for reading discomfort Spectacle, Magnifying SHIELD, EYE, OPHTHALMIC (INCLUDING SUNLAMP PROTECTIVE EYEWEAR AND POST-MYDRIATIC EYEWEAR) sunglasses Magnifier, Hand-Held, Low-Vision Lens, Spectacle, Non-custom(Prescription) Frame, Spectacle Lens, Spectacle, Non-custom(Prescription)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HJF Magnifier, Hand-Held, Low-Vision Ophthalmic Class 1 886.5540 2016-07-20
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2019-12-19
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2016-07-20
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2016-07-20

Official Correspondent

Nevies LEE

US Agent Details

Kevin Chao Email: kevin@contourop.com Phone: (425) 5919821

Related Public Records

Same Entity

AURORA OPTIC INC.
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 3013202270. Last updated year: 2026. Please use registration number 3013202270 when referencing this establishment in official correspondence.
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