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
2041102025
Device Listing 2041102025
Listing Summary
#
Listing key
2041102025
Premarket submission
K122325
Device
SKINTEMP II
Applicant
Human Biosciences, Inc.
Product code
KGN
Decision date
2012-10-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
346085
3042750477
3042750477
FR TECH, LLC
1
Y
2026-01-01
195 Advanced Dr Springboro OH US 45066