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
2054728780
Device Listing 2054728780
Listing Summary
#
Listing key
2054728780
Premarket submission
K241273
Device
FullFocus
Applicant
Paige.Ai, Inc.
Product code
QKQ
Decision date
2025-01-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
274691
3017125738
3017125738
PAIGE.AI, INC
1
N
2026-01-01
33 Irving Place 3rd Floor New York NY US 10003