JDDClass IIImplant

Prosthesis, Upper Femoral

Orthopedic · 21 CFR 888.3360

MDR events43All time

Recalls0All time

Registered firms3Currently listed

510(k) clearances0All time

Recent MDR events

43 adverse event reports on file

EXCEED ABT E1 N/FLNG CUP 28X48MMFeb 13, 2025
InjuryBiomet Uk Ltd.3002806535-2025-00023
EXCEED ABT E1 FLNG CUP 28X46MMApr 17, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00371
EXCEED ABT E1 N/FLNG CUP 32X50Mar 14, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00276
EXCEED ABT E1 FLNG CUP 32X52MMMar 14, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00283
EXCEED ABT E1 N/FLNG CUP 36X54Mar 13, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00268
EXCEED ABT E1 MULLER CUP 36X58Mar 13, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00269
EXCEED ABT E1 FLNG CUP 28X48MMMar 12, 2019
InjuryBiomet Uk Ltd.3002806535-2019-00262
THOMPSON ENDOPROSTHESIS 4 OF 6Jan 30, 2019
InjuryStryker Orthopaedics-mahwah0002249697-2019-00371
EXCEED ABT 3HL SHELL 44/56MMAug 30, 2018
InjuryBiomet Uk Ltd.3002806535-2018-01040
EXCEED ABT 3HL SHELL 48/60MMAug 29, 2018
InjuryBiomet Uk Ltd.3002806535-2018-01034

Event type breakdown

Injury40

Malfunction2

Other1

Most-reported manufacturers

Biomet Uk Ltd.10 Howmedica, Inc.6 Smith & Nephew, Inc., Orthopaedic Div.5 Zimmer4 Smith & Nephew Inc., Orthopaedic Div.2 Smith & Nephew, Inc., Orthopaedic Div2 Smith And Nephew, Inc2 Zimmer, Inc.2

Recalls

0 recall events for this product code

No recalls on file for this product code.

Registered firms

3 firms currently registered for this product code

510(k) clearances

0 clearances for this product code

No 510(k) clearances on file for this product code.