Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1176698663
Device Listing 1176698663
Listing Summary
#
Listing key
1176698663
Premarket submission
K973955
Device
HERNIAMESH SURGICAL MESHES
Applicant
Herniamesh
Product code
FTL
Decision date
1998-05-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
98145
9614846
3005404334
HERNIAMESH SRL
1
N
2026-01-01
Via Fratelli Meliga 1/c Chivasso Torino IT 10034