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
1413146028
Device Listing 1413146028
Listing Summary
#
Listing key
1413146028
Premarket submission
K230506
Device
PureLift Pro Edition
Applicant
Xtreem Pulse
Product code
NFO
Decision date
2023-06-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
219485
3012470925
3012470925
XTREEM PULSE
1
N
2026-01-01
690 Washington St # 4B New York NY US 10014