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
1150863470
Device Listing 1150863470
Listing Summary
#
Listing key
1150863470
Premarket submission
K203100
Device
Arthrex Eclipse Titanium Humeral Head
Applicant
Arthrex, Inc.
Product code
PKC
Decision date
2020-11-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
1476
1220246
1220246
ARTHREX, INC.
1
N
2026-01-01
1370 Creekside Blvd Naples FL US 34108
291362
3016851379
3016851379
Arthrex Distribution Hub EMEA B.V.
1
N
2026-01-01
Amperestraat 9 Venlo Limburg NL 5928 PE
296346
3020704423
3020704423
Barry Dietz
1
N
2026-01-01
1370 Creekside Blvd Naples FL US 34108