Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9614769

FEI Number

3002807499

Entity Name

LP ITALIANA SPA

City/State/Country

MILAN Milano, IT

Establishment Address

VIA CARLO REALE,15/4, 20157, MILAN Milano 19643204, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Polymedco, Inc. (Owner Number: 9011521)

Owner / Operator Contact Address

510 Furnace Dock Road, Cortlandt Manor, NY 10567, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SEDIMAT SEDITEN SEDIPLAST VENOPLAST

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GKB	Device, Automated Sedimentation Rate	Hematology	Class 1	864.5800	1995-05-19
JPH	Test, Erythrocyte Sedimentation Rate	Hematology	Class 1	864.6700	2011-07-26

Official Correspondent

Todd Kelley

US Agent Details

Todd Kelley Business: Polymedco Email: tkelley@polymedco.com Phone: (801) 8571609

Related Public Records

Same Entity

Polymedco, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9614769. Last updated year: 2026. Please use registration number 9614769 when referencing this establishment in official correspondence.