CHARMANT CO. LTD.

FDA Device Registration & Listing · ABERDEEN, HK · Registration 3003144305

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
3003144305
FEI Number
3003144305
Entity Name
CHARMANT CO. LTD.
City/State/Country
ABERDEEN, HK
Establishment Address
VITA TWR. 29 WONG CHUK HANG RD, 8/F-B, ABERDEEN --, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
CHARMANT CO. LTD. (Owner Number: 9051766)
Owner / Operator Contact Address
VITA TWR. 29 WONG CHUK HANG RD, 8/F-B, ABERDEEN, HK-NOTA --, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Charmant Charmant Charmant Isaac Mizrahi Eddie Bauer Elle Esprit Charmant Z-Titanium Ad-Lib Elle Charmant Titanium Minamoto Isaac Mizrahi Esprit Eddie Bauer Aristar

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2020-08-28
HPC Set, Lens, Trial, Ophthalmic Ophthalmic Class 1 886.1405 2018-07-18
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2010-10-22
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2002-06-19

Official Correspondent

No official correspondent registered.

US Agent Details

DOUGLASFRYER Business: CHARMANT USA Email: dfryer@charmant.com Phone: (973) 538

Related Public Records

Same Entity

CHARMANT 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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06
K900478 Woodlyn, Inc. WOODLYN FULL APERTURE TRIAL LENS SET 1990-02-21
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12

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3010141571 Xiantao Zhongyi Safety & Protection Products Co.,Ltd. Xiantao City Hubei, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003144305. Last updated year: 2026. Please use registration number 3003144305 when referencing this establishment in official correspondence.
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