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
1065254689
Device Listing 1065254689
Listing Summary
#
Listing key
1065254689
Premarket submission
K040019
Device
SILVERSEAL
Applicant
Noble Fiber Technologies
Product code
MGQ
Decision date
2004-07-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
263530
3016807311
3016807311
NEXGEL, INC.
1
N
2026-01-01
2150 Cabot Blvd W Suite B Langhorne PA US 19047