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Data / Medical devices / Italy / Herniamesh SRL

Herniamesh SRL: FDA-registered device maker in Chivasso Torino, Italy, 2 510(k) clearances

Herniamesh SRL is registered with the FDA (registration 9614846) in Chivasso Torino, Italy. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 19, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9614846
FEI number
3005404334
Address
Via Fratelli Meliga 1/c, Chivasso Torino, Italy, 10034
Owner or operator
HERNIAMESH SRL (10028147)
Roles
Manufacturer
First device listed
January 2, 2009
Registered through
2026
Brand names listed
Hertra 5, Hertra Kit, Hertra, Hertra 2, Hertra 2A, Hermesh, Plug T1, Plug T2, Plug T4, Net Plug & Patch, NeT Plug, Round Patch, Oval Patch,, Relimesh

Devices it lists

DeviceProduct codeClassRoleSource
Mesh, Surgical, PolymericFTL2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 19, 2008K081327RELIMESHFTLSubstantially EquivalentHerniamesh S.R.L.accessdata.fda.gov
May 11, 1998K973955HERNIAMESH SURGICAL MESHESFTLSubstantially EquivalentHerniameshaccessdata.fda.gov

Compare with other makers

Updated June 19, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.