Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014254835

FEI Number

3014254835

Entity Name

P L OVERSEAS LIMITED

City/State/Country

HONG KONG, HK

Establishment Address

FLAT / RM 1101 BLK 1 11F, CHEUNG SHA WAN PLAZA,, 833 CHEUNG SHA WAN ROAD, LAZ CHI KOK, HONG KONG 999077, HK

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

P L Overseas Limited (Owner Number: 10056522)

Owner / Operator Contact Address

FLAT/RM 1101 BLK 1 11F, CHEUNG SHA WAN PLAZA, 833 CHEUNG HSA WNA ROA, LAI CHI KOK, HONG KONG, HK-NOTA 999077, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172925

PMA Number

N/A

All Registered Proprietary Names

Contact Lens Case

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRX	Case, Contact Lens	Ophthalmic	Class 2	886.5928	2017-12-19

Official Correspondent

Hellen Ngan

US Agent Details

Alan Schwartz Business: mdi Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

P L Overseas Limited

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 3014254835. Last updated year: 2026. Please use registration number 3014254835 when referencing this establishment in official correspondence.