HERNIAMESH SRL

FDA Device Registration & Listing · Chivasso Torino, IT · Registration 9614846

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
9614846
FEI Number
3005404334
Entity Name
HERNIAMESH SRL
City/State/Country
Chivasso Torino, IT
Establishment Address
Via Fratelli Meliga 1/c, Chivasso Torino 10034, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HERNIAMESH SRL (Owner Number: 10028147)
Owner / Operator Contact Address
5 Wilder Lane, Huntington, NY 11743, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K973955
PMA Number
N/A

All Registered Proprietary Names

Hertra Kit Hertra, Hertra 2, Hertra 2A, Hermesh, Plug T1, Plug T2, Plug T4, Net Plug & Patch, NeT Plug, Round Patch, Oval Patch, Hertra 5

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTL Mesh, Surgical, Polymeric General, Plastic Surgery Class 2 878.3300 2009-01-02

Official Correspondent

No official correspondent registered.

US Agent Details

Lorena Trabucco Business: Herniamesh SRL Email: lorenat63@aol.com Phone: (516) 9879364

Related Public Records

Same Entity

HERNIAMESH 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
K220540 Covidien ProGrip Self-Gripping Polypropylene Mesh 2022-09-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9614846. Last updated year: 2026. Please use registration number 9614846 when referencing this establishment in official correspondence.
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