TAIZHOU RAPSON GLASSES CO.,LTD.

FDA Device Registration & Listing · Linhai Zhejiang, CN · Registration 3015009277

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
3015009277
FEI Number
3015009277
Entity Name
TAIZHOU RAPSON GLASSES CO.,LTD.
City/State/Country
Linhai Zhejiang, CN
Establishment Address
Banyang Village, Duqiao Town, Linhai Zhejiang 317016, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Taizhou Rapson Glasses Co., Ltd. (Owner Number: 10058720)
Owner / Operator Contact Address
Banyang Village, Duqiao Town, Linhai, CN-ZJ 317016, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Eye Shield Pill Organizer Reading Glasses Massager gun Medical Face Shield

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 2020-04-21
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2024-03-14
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2020-09-22
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-01-22
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-04-27

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Taizhou Rapson Glasses Co., 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
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015009277. Last updated year: 2026. Please use registration number 3015009277 when referencing this establishment in official correspondence.
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