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
2012170668
Device Listing 2012170668
Listing Summary
#
Listing key
2012170668
Premarket submission
K210191
Device
Identity Imprint Knee Replacement System
Applicant
Conformis, Inc.
Product code
JWH
Decision date
2021-05-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
183816
3004153240
3004153240
ConforMIS, Inc.
1
N
2026-01-01
600 Research Dr Wilmington MA US 01887