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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Super Search Devices@FDA
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New Search show TPLC since Back to Search Results
Device prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
Regulation Description Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.
Product CodeMBH
Regulation Number 888.3565
Device Class 2


Premarket Reviews
ManufacturerDecision
CONFORMIS INC
  SUBSTANTIALLY EQUIVALENT 1
CONFORMIS INC.
  SUBSTANTIALLY EQUIVALENT 1
DEPUY IRELAND UC
  SUBSTANTIALLY EQUIVALENT 6
ENCORE MEDICAL, L.P.
  SUBSTANTIALLY EQUIVALENT 1
ENCORE MEDICAL, L.P. DBA DJO SURGICAL
  SUBSTANTIALLY EQUIVALENT 1
EXACTECH INC.
  SUBSTANTIALLY EQUIVALENT 1
HOWMEDICA OSTEONICS CORP.
  SUBSTANTIALLY EQUIVALENT 1
LIMACORPORATE S.P.A.
  SUBSTANTIALLY EQUIVALENT 3
MAXX ORTHOPEDICS, INC.
  SUBSTANTIALLY EQUIVALENT 1
MEDACTA INTERNATIONAL S.A.
  SUBSTANTIALLY EQUIVALENT 2
MEDISURGE, LLC
  SUBSTANTIALLY EQUIVALENT 1
MICROPORT ORTHOPEDICS INC.
  SUBSTANTIALLY EQUIVALENT 2
OPTIMOTION IMPLANTS LLC
  SUBSTANTIALLY EQUIVALENT 1
OPTIMOTION IMPLANTS, LLC
  SUBSTANTIALLY EQUIVALENT 2
SIGNAL MEDICAL CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
SMITH & NEPHEW, INC.
  SUBSTANTIALLY EQUIVALENT 3
UNIK ORTHOPEDICS, INC.
  SUBSTANTIALLY EQUIVALENT 1
UNITED ORTHOPEDIC CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
WALDEMAR LINK GMBH & CO. KG
  SUBSTANTIALLY EQUIVALENT 2
ZIMMER BIOMET
  SUBSTANTIALLY EQUIVALENT 1
ZIMMER, INC.
  SUBSTANTIALLY EQUIVALENT 4

MDR Year MDR Reports MDR Events
2020 1089 1089
2021 1539 1539
2022 1260 1260
2023 1267 1267
2024 1494 1494
2025 203 203

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 2544 2544
Fracture 884 884
Unstable 743 743
Insufficient Information 549 549
Loss of Osseointegration 311 311
Break 310 310
Loosening of Implant Not Related to Bone-Ingrowth 187 187
Detachment of Device or Device Component 182 182
Difficult to Insert 178 178
Naturally Worn 144 144
Osseointegration Problem 133 133
Migration 118 118
Device Dislodged or Dislocated 112 112
Degraded 101 101
Mechanical Problem 76 76
Noise, Audible 74 74
Malposition of Device 72 72
Positioning Failure 59 59
Loss of or Failure to Bond 52 52
Material Erosion 51 51
Use of Device Problem 50 50
Unintended Movement 48 48
Loose or Intermittent Connection 47 47
Patient Device Interaction Problem 47 47
Connection Problem 46 46
Material Deformation 44 44
Appropriate Term/Code Not Available 38 38
Crack 29 29
Dull, Blunt 29 29
Mechanical Jam 22 22
Inadequacy of Device Shape and/or Size 21 21
Component Missing 20 20
Packaging Problem 19 19
Incomplete or Inadequate Connection 17 17
Device Contaminated During Manufacture or Shipping 17 17
Corroded 16 16
Off-Label Use 16 16
Tear, Rip or Hole in Device Packaging 15 15
Device-Device Incompatibility 14 14
Device Damaged Prior to Use 13 13
Material Fragmentation 13 13
Failure to Osseointegrate 13 13
Device Difficult to Setup or Prepare 12 12
Contamination /Decontamination Problem 10 10
Fitting Problem 10 10
Device Markings/Labelling Problem 8 8
Device Reprocessing Problem 8 8
Defective Device 8 8
Improper or Incorrect Procedure or Method 8 8
Material Integrity Problem 8 8

Patient Problems MDRs with this Patient Problem Events in those MDRs
Pain 1623 1623
No Clinical Signs, Symptoms or Conditions 1476 1476
Unspecified Infection 747 747
Joint Laxity 665 665
Insufficient Information 596 596
Loss of Range of Motion 577 577
Ambulation Difficulties 434 434
Inadequate Osseointegration 379 379
Injury 350 350
Failure of Implant 321 321
Swelling/ Edema 320 320
Scar Tissue 208 208
Bone Fracture(s) 179 179
Fall 169 169
Adhesion(s) 125 125
No Known Impact Or Consequence To Patient 110 110
No Patient Involvement 88 88
Inflammation 78 78
No Consequences Or Impact To Patient 76 76
Joint Dislocation 71 71
Muscular Rigidity 68 68
Thrombosis/Thrombus 54 54
Discomfort 53 53
Muscle/Tendon Damage 52 52
No Information 52 52
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 50 50
Fibrosis 43 43
Osteolysis 41 41
Unspecified Tissue Injury 41 41
Limited Mobility Of The Implanted Joint 38 38
Swelling 38 38
Damage to Ligament(s) 35 35
Hypersensitivity/Allergic reaction 34 34
Synovitis 33 33
Bacterial Infection 32 32
Numbness 28 28
Hematoma 26 26
Wound Dehiscence 24 24
Impaired Healing 21 21
Nerve Damage 21 21
Foreign Body Reaction 21 21
Fluid Discharge 20 20
Aspiration/Inhalation 20 20
Implant Pain 20 20
No Code Available 19 19
Necrosis 19 19
Cyst(s) 19 19
Embolism 19 19
Metal Related Pathology 18 18
Subluxation 17 17

Recalls
Manufacturer Recall Class Date Posted
1 Biomet, Inc. II Apr-22-2024
2 Biomet, Inc. II Oct-08-2020
3 Biomet, Inc. II May-28-2020
4 DePuy Orthopaedics, Inc. II Mar-29-2024
5 Encore Medical, LP II Dec-07-2023
6 Encore Medical, LP II Nov-07-2023
7 Encore Medical, LP II Apr-12-2023
8 Encore Medical, LP II Oct-07-2020
9 Howmedica Osteonics Corp. II Mar-06-2024
10 Howmedica Osteonics Corp. II May-30-2023
11 Howmedica Osteonics Corp. II Mar-08-2021
12 MicroPort Orthopedics Inc. II Dec-18-2024
13 Smith & Nephew, Inc. II Jan-28-2020
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