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
1869272924
Device Listing 1869272924
Listing Summary
#
Listing key
1869272924
Premarket submission
K992298
Device
IRIDERM, MODEL APEX 800
Applicant
Iridex Corp
Product code
GEX
Decision date
1999-12-09
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