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
1372496104
Device Listing 1372496104
Listing Summary
#
Listing key
1372496104
Premarket submission
K212731
Device
Circul8 Pro
Applicant
Ortho8, Inc.
Product code
JOW
Decision date
2021-11-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
302549
3016000973
3016000973
Precision Medical Products
1
Y
2026-01-01
3735 Cincinnati Ave Ste 100 Rocklin CA US 95765