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
1078046332
Device Listing 1078046332
Listing Summary
#
Listing key
1078046332
Premarket submission
K110427
Device
FEMTEC LASER SYSTEM FOR CAPSULOTOMY
Applicant
Technolas Perfect Vision GmbH
Product code
OOE
Decision date
2011-11-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
103543
3007606649
3003691824
Margaret Wood
1
N
2026-01-01
400 Somerset Corporate Blvd. -- Bridgewater NJ US 08807