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
1744263636
Device Listing 1744263636
Listing Summary
#
Listing key
1744263636
Premarket submission
K193426
Device
Elite iQ
Applicant
Cynosure, LLC
Product code
GEX
Decision date
2020-03-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
62269
3001431138
3001431138
Greg Swanson
1
N
2026-01-01
2500 Bee Cave Rd. Bldg. 1, Ste. 300 Austin TX US 78746