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
1043048539
Device Listing 1043048539
Listing Summary
#
Listing key
1043048539
Premarket submission
K113857
Device
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE
Applicant
Synergetics, Inc.
Product code
HQB
Decision date
2012-04-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
45717
1932402
1000119053
SYNERGETICS, INC.
1
Y
2026-01-01
3845 Corporate Centre Dr O Fallon MO US 63368