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
1203731509
Device Listing 1203731509
Listing Summary
#
Listing key
1203731509
Premarket submission
K203282
Device
TECHFIT Patient-Specific Maxillofacial System
Applicant
Industrias Medicas Sampedro S.A.S
Product code
JEY
Decision date
2021-05-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
43243
3025141
1000125930
ACUMED LLC
1
Y
2026-01-01
5885 NE Cornelius Pass Rd Hillsboro OR US 97124