LANGFANG FAR EAST PROSPEROUS OPTICAL INSTRUMENT CO.,LTD.

FDA Device Registration & Listing · Langfang Hebei, CN · Registration 3008197763

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
3008197763
FEI Number
3008197763
Entity Name
LANGFANG FAR EAST PROSPEROUS OPTICAL INSTRUMENT CO.,LTD.
City/State/Country
Langfang Hebei, CN
Establishment Address
Xinyuan Road Development Zone, Langfang Hebei 065001, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LangFang Far East Prosperous Optical Instrument Co.,Ltd. (Owner Number: 10089064)
Owner / Operator Contact Address
Xinyuan Road Development Zone, Langfang, CN-HE 065001, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Internal illuminated Chart projects Chart projects Trial case lenses Ophthalmic instrument tables LCD Visual Chart Refractor heads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOS Projector, Ophthalmic Ophthalmic Class 1 886.1680 2023-11-03
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2023-11-03
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 2023-11-03
QTO Digital Visual Acuity Test Ophthalmic Class 1 886.1150 2023-11-03
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2023-11-03

Official Correspondent

Huaiyu Deng

US Agent Details

hui hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (303) 8000162

Related Public Records

Same Entity

LangFang Far East Prosperous Optical Instrument 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
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21

Similar Registrations

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3009515444 GINO OPTICAL (SHANGHAI) CO., LTD. Shanghai, CN
3033566 OCULUS, INC. Arlington, WA, US
3015972897 INNOVA MEDICAL OPHTHALMICS Toronto Ontario, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008197763. Last updated year: 2026. Please use registration number 3008197763 when referencing this establishment in official correspondence.
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