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
1348105776
Device Listing 1348105776
Listing Summary
#
Listing key
1348105776
Premarket submission
K984443
Device
ORBSCAN
Applicant
Technolas Perfect Vision GmbH
Product code
MXK
Decision date
1999-03-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
26861
1920664
1920664
Bausch & Lomb Incorporated
1
Y
2026-01-01
3365 TREE CT. INDUSTRIAL BLVD. Saint Louis MO US 63122