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
1377045863
Device Listing 1377045863
Listing Summary
#
Listing key
1377045863
Premarket submission
K201393
Device
restor3d MTP Implant
Applicant
Restor3D, Inc.
Product code
KWD
Decision date
2022-05-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
221234
3014833750
3014833750
restor3d, inc.
1
N
2026-01-01
4001 NC Hwy 54, Suite 2160 Durham NC US 27709