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
1513275767
Device Listing 1513275767
Listing Summary
#
Listing key
1513275767
Premarket submission
K242818
Device
IsoSphere
Applicant
Isoaid, LLC
Product code
KXK
Decision date
2025-07-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
59948
3003440305
3003440305
ISOAID, L.L.C.
1
N
2026-01-01
7824 CLARK MOODY BLVD. PORT RICHEY FL US 34668