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
1541544313
Device Listing 1541544313
Listing Summary
#
Listing key
1541544313
Premarket submission
K230850
Device
United Orthopedic Knee Patient Specific Instrumentation
Applicant
Enhatch, Inc.
Product code
OOG
Decision date
2023-12-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
324894
3030409224
3030409224
ENHATCH, INC
1
N
2026-01-01
411 State Rt 17 Ste 500 Hasbrouck Heights NJ US 07604