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
1503287004
Device Listing 1503287004
Listing Summary
#
Listing key
1503287004
Premarket submission
K260381
Device
Eve
Applicant
Wandercraft SAS
Product code
PHL
Decision date
2026-08-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
315004
3015000676
3015000676
WANDERCRAFT
1
N
2026-01-01
23-23 bis avenue d'Italie Paris Ile-de-France FR 75013
334719
3034724466
3034724466
Wandercraft Incorporated
1
N
2026-01-01
345 Park Ave S New York NY US 10010