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
1961538724
Device Listing 1961538724
Listing Summary
#
Listing key
1961538724
Premarket submission
K122829
Device
LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS
Applicant
Lensar, Inc.
Product code
HQC
Decision date
2012-12-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
142439
3009026057
3009026057
LENSAR, Inc
1
N
2026-01-01
2800 Discovery Drive Suite 100 Orlando FL US 32826