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
1796203417
Device Listing 1796203417
Listing Summary
#
Listing key
1796203417
Premarket submission
DEN180060
Device
Plenity
Applicant
Gelesis, Inc.
Product code
QFQ
Decision date
2019-04-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
230603
3012121187
3012121187
GELESIS SRL
1
N
2026-01-01
Via Europa, 187 Calimera Lecce IT 73021