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
1013746896
Device Listing 1013746896
Listing Summary
#
Listing key
1013746896
Premarket submission
K173544
Device
Phoenix Wound Matrix
Applicant
Nanofiber Solutions, Inc.
Product code
QSZ
Decision date
2018-03-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
217348
3014527904
3014527904
NANOFIBER SOLUTIONS LLC
1
N
2026-01-01
5164 Blazer Parkway Dublin OH US 43017