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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device needle, dental
Product CodeDZM
Regulation Number 872.4730
Device Class 1

MDR Year MDR Reports MDR Events
2017 25 25
2018 38 38
2019 31 31
2020 16 16
2021 41 65
2022 35 35
2023 34 34
2024 6 6

Device Problems MDRs with this Device Problem Events in those MDRs
Break 105 117
Detachment of Device or Device Component 36 36
Material Fragmentation 36 39
Material Separation 15 17
Fitting Problem 9 9
Material Puncture/Hole 8 8
Loose or Intermittent Connection 6 6
Disconnection 5 5
Entrapment of Device 5 5
Product Quality Problem 5 5
Adverse Event Without Identified Device or Use Problem 4 4
Leak/Splash 4 4
Device Contamination with Chemical or Other Material 3 3
Detachment Of Device Component 3 3
Fluid/Blood Leak 3 7
Device Contamination with Body Fluid 3 7
Bent 3 3
Difficult to Remove 2 2
Material Twisted/Bent 2 2
Material Integrity Problem 2 2
Connection Problem 2 2
Fail-Safe Problem 1 1
Use of Device Problem 1 1
Device Dislodged or Dislocated 1 1
Loss of or Failure to Bond 1 1
Fail-Safe Did Not Operate 1 1
Defective Component 1 1
Sticking 1 1
Unintended Movement 1 1
Device Handling Problem 1 2
Material Protrusion/Extrusion 1 1
Off-Label Use 1 3

Patient Problems MDRs with this Patient Problem Events in those MDRs
Device Embedded In Tissue or Plaque 92 100
Foreign Body In Patient 59 73
Needle Stick/Puncture 40 45
Exposure to Body Fluids 31 31
No Consequences Or Impact To Patient 16 16
No Known Impact Or Consequence To Patient 9 9
No Clinical Signs, Symptoms or Conditions 9 9
Pain 7 7
No Code Available 5 5
No Information 4 4
Necrosis 3 3
Hemorrhage/Bleeding 2 2
Unspecified Tissue Injury 2 2
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Peripheral Nervous Injury 1 1
Pyogenic Infection 1 1
Inflammation 1 1
Foreign Body Reaction 1 1
Ulcer 1 1
Discomfort 1 1
Injury 1 1
No Patient Involvement 1 1

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