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
1826916758
Device Listing 1826916758
Listing Summary
#
Listing key
1826916758
Premarket submission
K253884
Device
Koios DS (3.8)
Applicant
Koios Medical, Inc.
Product code
POK
Decision date
2026-07-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
206649
3010119782
3010119782
Koios Medical, Inc.
1
N
2026-01-01
242 West 38th Street 14th Floor New York NY US 10018