Anco China Ltd

FDA Device Registration & Listing · Hong Kong, CN · Registration 3011803475

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
3011803475
FEI Number
3011803475
Entity Name
Anco China Ltd
City/State/Country
Hong Kong, CN
Establishment Address
5/F Lippo Leighton Tower, 103-109 Leighton Road, Causeway Bay, Hong Kong Hong Kong, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
IF USA, LLC (Owner Number: 10049229)
Owner / Operator Contact Address
4350 Bryson Blvd, Florence, AL 35630, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Skinny Readers Handy Specs Spare Pair Compact Lenses Shhh! Foam Earplugs Compact Lenses Light-Up Readers Pocket Readers Really Tiny Quick Specs Skinny Readers Bookaroo Handy Specs Inspectors Make Up Glasses Spare Pair Easy Readers - Book Lover's Spare Pair Night Readers Peggy's Baking Glasses Easy Readers Reading Glasses Magnif-i - Hobby Glasses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2015-04-30
EWD Protector, Hearing (Insert) Unknown Class U N/A 2018-07-20
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2015-04-30

Official Correspondent

Cherrain Bailey

US Agent Details

Cherrain Bailey Business: IF USA, LLC Email: Cherrain.Bailey@ifplc.com Phone: (866) 7296160

Related Public Records

Same Entity

IF USA, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004061392 If Cardboard Creations Limited Pickering North Yorkshire, GB
3011592852 IF USA, LLC Florence, AL, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011803475. Last updated year: 2026. Please use registration number 3011803475 when referencing this establishment in official correspondence.
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