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
1016337343
Device Listing 1016337343
Listing Summary
#
Listing key
1016337343
Premarket submission
K220523
Device
restor3d TiDAL Lumbar Interbody Fusion Device
Applicant
Restor3D
Product code
MAX
Decision date
2022-06-17
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