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
2031367644
Device Listing 2031367644
Listing Summary
#
Listing key
2031367644
Premarket submission
K191086
Device
Exciplex
Applicant
Clarteis
Product code
FTC
Decision date
2019-12-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
20233
3004374705
3004374705
AEROLASE CORPORATION
1
N
2026-01-01
120 White Plains Road SUITE 515 Tarrytown NY US 10591