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
1381430993
Device Listing 1381430993
Listing Summary
#
Listing key
1381430993
Premarket submission
K062369
Device
IRIDEX OCULIGHT TX
Applicant
Iridex Corp
Product code
GEX
Decision date
2006-11-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
43232
2939653
2939653
Iridex Corporation
1
N
2026-01-01
1212 Terra Bella Avenue MOUNTAIN VIEW CA US 94043