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
1982496457
Device Listing 1982496457
Listing Summary
#
Listing key
1982496457
Premarket submission
K210166
Device
Omnispec ED1000
Applicant
Medispec, Ltd.
Product code
ISA
Decision date
2023-01-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
61613
3004167969
3004167969
ALMA LASERS LTD.
1
N
2026-01-01
18 Haharash Street NORTH INDUSTRIAL PARK CAESAREA Northern IL 3079895