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
1155843908
Device Listing 1155843908
Listing Summary
#
Listing key
1155843908
Premarket submission
K972661
Device
EYE SPHERE, CONFORMERS
Applicant
Gulden Ophthalmics
Product code
HPZ
Decision date
1997-10-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72383
2518410
2518410
GULDEN OPHTHALMICS
1
N
2026-01-01
225 CADWALADER AVE. Elkins Park PA US 19027