AGRITALIA SPA

FDA Device Registration & Listing · ISOLA E2 Napoli, IT · Registration 1000508490

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
1000508490
FEI Number
1000508490
Entity Name
AGRITALIA SPA
City/State/Country
ISOLA E2 Napoli, IT
Establishment Address
CENTRO DIREZIONALE ISOLA E2, ISOLA E2 Napoli 80143, IT
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
AGRITALIA SRL (Owner Number: 10080885)
Owner / Operator Contact Address
CENTRO DIREZIONALE ISOLA E2, ISOLA E2, IT-NA 80143, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DENTAL FLOSS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JES Floss, Dental Dental Class 1 872.6390 2021-03-04

Official Correspondent

CHAIARA LA MARCA

US Agent Details

Shawn Barnes Business: ALL-WAYS FORWARDING INT'L INC. Email: SHAWN.BARNES@SHIPALLWAYS.COM Phone: (908) 3534000

Related Public Records

Same Entity

AGRITALIA 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
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

Similar Registrations

Registration Number Establishment Name Location
3016396121 CONVII INC Santa Clara, CA, US
3007420842 Hebei Fenghe Biotechnology INC.,Ltd Handan Hebei, CN
3033258462 ANQING GEHENG E-COMMERCE CO., LTD. Anqing Anhui, CN
3014045831 DENTAL LACE INC. Pittsfield, ME, US
3038200340 WEIFANG YANGXU LABOR PROTECTION PRODUCTS CO., LTD Weifang Shandong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000508490. Last updated year: 2026. Please use registration number 1000508490 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.