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
1838176444
Device Listing 1838176444
Listing Summary
#
Listing key
1838176444
Premarket submission
K990032
Device
MODULAR PROTUSIO CUP
Applicant
Biomet, Inc.
Product code
JDI
Decision date
1999-02-18
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
108775
3007923096
3007923096
Changzhou Biomet Medical Devices Co., Ltd.
1
N
2026-01-01
No. 235 Chuangxin Road EPZ Xinbei District Changzhou City Jiangsu CN 213031