Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008309596

FEI Number

3008309596

Entity Name

Two B srl

City/State/Country

Quero Vas Belluno, IT

Establishment Address

Via Andrea Redusio 14/B, Quero Vas Belluno 32038, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Two B s.r.l. (Owner Number: 10031845)

Owner / Operator Contact Address

Via Andrea Redusio 14/B, Setteville, IT-BL 32038, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KIRKLAND SIGNATURE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2010-03-15

Official Correspondent

Elena Berton

US Agent Details

Lisa Wright Business: THE VISION COUNCIL Email: fda@thevisioncouncil.org Phone: (703) 5484560

Related Public Records

Same Entity

Two B s.r.l.

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

Similar Registrations

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3007521479	NY2LA INC.	Camarillo, CA, US
3005147601	VISIONTECH EXPORT INTERNATIONAL (PVT) LTD.	KARACHI Sindh, PK
3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
3013507321	DEM FACTORY S.R.L.	Limana Belluno, IT
3015243992	L.G.R SRL	Roma, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008309596. Last updated year: 2026. Please use registration number 3008309596 when referencing this establishment in official correspondence.