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
1658157864
Device Listing 1658157864
Listing Summary
#
Listing key
1658157864
Premarket submission
K032401
Device
ORTHOVIEW
Applicant
Omsbar, Ltd.
Product code
LLZ
Decision date
2003-08-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
80923
3004537781
3004537781
MERIDIAN TECHNIQUE LTD
1
N
2026-01-01
Epsilon House, Enterprise Road SOUTHAMPTON SCIENCE PARK SOUTHAMPTON Hampshire GB SO16 7NS