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
2026627592
Device Listing 2026627592
Listing Summary
#
Listing key
2026627592
Premarket submission
K151601
Device
SECURE-LOOP
Applicant
Xiros, Ltd.
Product code
MBI
Decision date
2015-09-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
42825
8044102
3013299874
XIROS LTD
1
N
2026-01-01
SPRINGFIELD HOUSE WHITEHOUSE LANE YEADON Leeds GB LS19 7UE