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
1446132305
Device Listing 1446132305
Listing Summary
#
Listing key
1446132305
Premarket submission
K925015
Device
STERILE SUTURE REMOVAL KIT
Applicant
Customed, Inc.
Product code
MCZ
Decision date
1993-06-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
42582
2648727
2648727
CUSTOMED, INC.
1
Y
2026-01-01
CALLE IGUALDAD No. 7 Fajardo PR US 00738