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
1664720569
Device Listing 1664720569
Listing Summary
#
Listing key
1664720569
Premarket submission
K171356
Device
Clarity Reveal
Applicant
Ceevra, Inc.
Product code
LLZ
Decision date
2017-08-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
213029
3014132130
3014132130
CEEVRA, INC.
1
N
2026-01-01
465 California St Fl 7 San Francisco CA US 94104