Skip to content

Herniamesh S.r.l.

Country not established

Devices
2

What Herniamesh S.r.l. makes

Herniamesh S.R.L. manufactures surgical mesh products, including the T-SLING for hernia repair and the RELIMESH for tissue reinforcement in abdominal wall procedures. These devices are designed for use in minimally invasive and open surgical techniques to support tissue integrity and promote healing.

The company’s portfolio is classified under FDA Class II devices and is listed via 510(k) premarket notifications. Herniamesh S.R.L. is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • T-Sling Ref K050516

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Relimesh Ref K081327

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

Frequently asked questions

How many devices does Herniamesh S.R.L. have in the registry?

The registry currently lists 2 devices for Herniamesh S.R.L.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Herniamesh S.R.L.'s devices?

Among its 2 most recently registered devices, Herniamesh S.R.L. has devices listed in FDA 510(k) (2 devices).

What risk classes do Herniamesh S.R.L.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Herniamesh S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Herniamesh S.R.L. in the registry?

The most recently registered devices listed for Herniamesh S.R.L. include T-SLING and RELIMESH.

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