Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043648613

FEI Number

3043648613

Entity Name

LINHAI PENGTAI GLASSES CO., LTD.

City/State/Country

Taizhou Zhejiang, CN

Establishment Address

No. 1-28, East Room, Building 3, Duqiao Glasses City, Duqiao Town, Linhai City, Taizhou Zhejiang 318000, CN

Establishment Type(s)

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

Owner / Operator

Linhai Pengtai Glasses Co., Ltd. (Owner Number: 10094984)

Owner / Operator Contact Address

No. 1-28, East Room, Building 3, Duqiao Glasses City, Duqiao Town, Linhai City, Taizhou, CN-ZJ 318000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

goggles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2026-01-12

Official Correspondent

Yiming Yang

US Agent Details

James St. Wu Business: Humiss Inc. Email: fda-reg@humiss.com Phone: (720) 7595888

Related Public Records

Same Entity

Linhai Pengtai Glasses Co., Ltd.

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 3043648613. Last updated year: 2026. Please use registration number 3043648613 when referencing this establishment in official correspondence.