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
1482744176
Device Listing 1482744176
Listing Summary
#
Listing key
1482744176
Premarket submission
K231838
Device
RxSight® Insertion Device (63002)
Applicant
Rxsight, Inc.
Product code
MSS
Decision date
2023-08-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
195306
3012712027
3012712027
RxSight Inc.
1
N
2026-01-01
100 Columbia Aliso Viejo CA US 92656