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
1647166643
Device Listing 1647166643
Listing Summary
#
Listing key
1647166643
Premarket submission
K121272
Device
PROTECH DENT
Applicant
Akervall Technologies, Inc.
Product code
OBR
Decision date
2012-10-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
181475
3011547262
3011547262
AKERVALL TECHNOLOGIES
1
N
2026-01-01
1512 Woodland Dr Saline MI US 48176