Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8021022

FEI Number

7163

Entity Name

NANNINI ITALIAN QUALITY SRL

City/State/Country

REGGIO EMILIA, IT

Establishment Address

VIA J.F.KENNEDY, 10, REGGIO EMILIA 42124, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

NANNINI ITALIAN QUALITY SRL (Owner Number: 8021022)

Owner / Operator Contact Address

VIA J.F. KENNEDY, 10, --, REGGIO EMILIA, IT-RE 42124, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NANNINI NANNINI NANNINI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	1995-08-16
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	1985-06-13
HQY	Sunglasses (Non-Prescription Including Photosensitive)	Ophthalmic	Class 1	886.5850	1985-06-13

Official Correspondent

LORENZO MONTICELLI

US Agent Details

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

Related Public Records

Same Entity

NANNINI ITALIAN QUALITY SRL

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
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

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3000180670	Dongguan Rijinyuehui Optical Co.,Ltd	Dongguan Guangdong, CN
3009206998	WORLDWIDE PACKAGING, INC	Livermore, CA, US
3013009176	HYUNDAI SAFETYWEAR CO.	Tainan City, TW

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8021022. Last updated year: 2026. Please use registration number 8021022 when referencing this establishment in official correspondence.