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
1420221541
Device Listing 1420221541
Listing Summary
#
Listing key
1420221541
Premarket submission
K183458
Device
exoplan 2.3
Applicant
Exocad GmbH
Product code
LLZ
Decision date
2019-08-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
208955
3011521456
3011521456
Mary Collington
1
N
2026-01-01
301 Edgewater Pl Ste 330 Wakefield MA US 01880
209813
3013718526
3013718526
EXOCAD AMERICA, INC.
1
Y
2026-01-01
301 Edgewater Pl Ste 330 Wakefield MA US 01880