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
2045422251
Device Listing 2045422251
Listing Summary
#
Listing key
2045422251
Premarket submission
K011138
Device
OXFORD UNICOMPARTMENTAL KNEE FEMORAL COMPONENT
Applicant
Biomet, Inc.
Product code
HRY
Decision date
2001-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3946
1825034
1825034
BIOMET, INC.
1
Y
2026-01-01
56 E Bell Dr Po Box 587 WARSAW IN US 46581
164994
9610918
3002806539
Biomet UK Ltd
1
N
2020-04-25
Dorcan One Hundred Murdock Road Dorcan Industrial Estate Swindon Wiltshire GB SN3 5HY