LARA D SRL

FDA Device Registration & Listing · BELLUNO, IT · Registration 3011689636

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
3011689636
FEI Number
3011689636
Entity Name
LARA D SRL
City/State/Country
BELLUNO, IT
Establishment Address
VIA ROMA 3, TRICHIANA, BELLUNO 32026, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LARA D SRL UNIPERSONALE (Owner Number: 10049682)
Owner / Operator Contact Address
VIA ROMA 3, TRICHIANA, BELLUNO, IT-BL 32026, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lara D

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2015-07-09

Official Correspondent

LARA D'ALPAOS

US Agent Details

Caterina Zimmerman Business: Pangea Export USA LLC Email: info@pangeaexport.us Phone: (415) 2506061

Related Public Records

Same Entity

LARA D SRL UNIPERSONALE
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
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 3011689636. Last updated year: 2026. Please use registration number 3011689636 when referencing this establishment in official correspondence.
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