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
1445044640
Device Listing 1445044640
Listing Summary
#
Listing key
1445044640
Premarket submission
K943492
Device
ARTHREX STAPLES
Applicant
Arthrex, Inc.
Product code
JDR
Decision date
1995-02-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
298616
3003755939
3003755939
Barry Dietz
1
N
2026-01-01
1370 Creekside Blvd Naples FL US 34108