Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008517911

FEI Number

3008517911

Entity Name

PILOT OPTICS INTERNATIONAL CORP. LTD. WENZHOU

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

NO.38 QianJiang Road,Puzhou Sub-district,Longwan District,, Wenzhou Zhejiang 325000, CN

Establishment Type(s)

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

Owner / Operator

Pilot Optics International Corp. Ltd. Wenzhou (Owner Number: 10033334)

Owner / Operator Contact Address

NO.38 QianJiang Road,Puzhou Sub-district,Longwan District,, Wenzhou, CN-ZJ 325000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Reading Glasses Shield Eye Ophthalmic Safety Glasses, Goggles Mask Face Mask, Disposable Medical Mask, Face Shield, Mask

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2010-08-04
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2020-03-18
KHA	Mask, Scavenging	Anesthesiology	Class 1	868.5590	2020-03-18
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2020-03-18
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2019-05-21

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

Pilot Optics International Corp. Ltd. Wenzhou

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 3008517911. Last updated year: 2026. Please use registration number 3008517911 when referencing this establishment in official correspondence.