Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009005492

FEI Number

3009005492

Entity Name

Activation Eyewear Corp

City/State/Country

Taizhou Zhejiang, CN

Establishment Address

Building 12 NO.24, Yaoda, Duqiao Town,, Taizhou Zhejiang 317016, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Activation Eyewear Corp (Owner Number: 10039722)

Owner / Operator Contact Address

Building 12 NO.24, Yaoda, Duqiao Town,, Linhai, CN-ZJ 317016, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SUNGLASSES READING GLASSES OPTICAL FRAME

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQY	Sunglasses (Non-Prescription Including Photosensitive)	Ophthalmic	Class 1	886.5850	2012-02-06
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2012-02-06
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2012-02-06

Official Correspondent

No official correspondent registered.

US Agent Details

Kai Li Email: likai323@hotmail.com Phone: (501) 7778490

Related Public Records

Same Entity

Activation Eyewear 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
K940726	Jay-Y Enterprises Co., Inc.	NONE-GENERIC	1994-04-11
K934837	Simon Marketing, Inc.	SUNGLASSES	1993-12-08
K852902	Yours Enterprise Co., Ltd.	METALLIC SUNGLASSES	1985-08-12
K970895	Custom Optical Frames, Inc.	CUSTOM OPTICAL SUNGLASS FRAMES	1997-05-06
K853921	Winsburn Company , Ltd.	ALL KINDS OF SUNGLASSES	1985-10-15

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3009141079	STAGE	Sandy, UT, US
3013857947	FARFETCH ITALIA S.R.L.	MILAN Milano, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009005492. Last updated year: 2026. Please use registration number 3009005492 when referencing this establishment in official correspondence.