Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012583348

FEI Number

3012583348

Entity Name

ADALCA STUDIO LLC

City/State/Country

Fort Lauderdale, FL, US

Establishment Address

1919 NE 45th Street Ste 122, Fort Lauderdale, FL 33308, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Adalca Studio LLC (Owner Number: 10052114)

Owner / Operator Contact Address

1919 NE 45TH STREET SUITE 122, Fort Lauderdale, FL 33308, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

OPTA FILAO CAROLINE ABRAM LUNETTES GLG EYEWEAR TALLA EYEWEAR GLG EYEWEAR TALLA EYEWEAR OPTA FILAO CAROLINE ABRAM LUNETTES

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQY	Sunglasses (Non-Prescription Including Photosensitive)	Ophthalmic	Class 1	886.5850	2023-11-10
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2023-11-10

Official Correspondent

Samia Beddar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Adalca Studio LLC

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
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
K970895	Custom Optical Frames, Inc.	CUSTOM OPTICAL SUNGLASS FRAMES	1997-05-06
K853921	Winsburn Company , Ltd.	ALL KINDS OF SUNGLASSES	1985-10-15

Similar Registrations

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3042870833	GOLEADER(VIETNAM) RECREATION LIMITED	Tan Phuoc 3 Commune Dong Thap, VN
3009141079	STAGE	Sandy, UT, US
3013857947	FARFETCH ITALIA S.R.L.	MILAN Milano, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012583348. Last updated year: 2026. Please use registration number 3012583348 when referencing this establishment in official correspondence.