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Herniamesh

Also registered as HERNIAMESH SRL

Country not established FDA

Herniamesh is a medical device manufacturer, with 60 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.

Devices
60
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 58
  • FDA 510(k) 2

A device listed in two registries counts in both.

Device classes
  • FDA Class II 60

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Herniamesh makes

Herniamesh manufactures synthetic polymer surgical meshes for extra-gynaecological applications, including products like the HERMESH line and PLUG T-series implants. The portfolio also includes the HERTRA kit and variants for hernia repair. These devices are designed for permanent implantation to support tissue reinforcement in abdominal and pelvic regions.

The company’s products are classified as Class II medical devices under FDA regulations and are authorised via 510(k) clearances and the Unique Device Identifier (UDI) system. These devices are listed in the FDA’s regulatory databases, and Herniamesh operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue60

Newest first, rows 1-50 of 60

Search and filter all 60 devices
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  • Hermesh H41515

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T2 PT2/3

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H60611

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H40815

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra Kit H1T25

    Active Regimes: 510(k) Registry: GUDID Class:II
  • T-Sling 5194001400

    Withdrawn Registry: GUDID Class:II
  • Hertra HTR9A511

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra 2A HTR2A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra HTR09

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T1 PT1/5

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H91515

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H93030

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T4 PT4R-S

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra HTR9A

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra HTR90511

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T2 PT2/3-H3

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H30611

    Listed Registry: GUDID Class:II
  • Hermesh H40611

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H61015

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra 5 HTR05

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H40530

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H90815

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra HTR60513

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H60815

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H50611

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T2 PT2/7-H3

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T4 PT4R-Q

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Net Plug & Patch PT3H3PS-P

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Oval Patch OP1114

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Relimesh PEP1418-O

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra HTR90513

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H91015

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H43030

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra Kit H2T25

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Round Patch HT1C10

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H95050

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra 2 HTR02

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H90611

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H61515

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra 5 HTR50513

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T4 PT4R-R

    Withdrawn Registry: GUDID Class:II
  • Hermesh H31515

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hertra Kit H1T27

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H105050

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Plug T5 PT50-S

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Net Plug PT2/6-P

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H51515

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H40210

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Hermesh H42020

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Round Patch H5C10

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 60

Showing 1-50 of 60

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Herniamesh SRL Chivasso Torino · IT FEI 3005404334

Frequently asked questions

How many devices does Herniamesh have in the registry?

The registry currently lists 60 devices for Herniamesh. Devices recorded under merged duplicate company entries are counted once.

Which registries list Herniamesh's devices?

Among its 50 most recently registered devices, Herniamesh has devices listed in FDA GUDID (50 devices).

What risk classes do Herniamesh's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Herniamesh's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Herniamesh in the registry?

The most recently registered devices listed for Herniamesh include HERMESH H41515, PLUG T2 PT2/3, HERMESH H60611 and HERMESH H40815.

Which FDA establishments are linked to Herniamesh?

1 FDA establishment is linked to Herniamesh in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.