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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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New Search show TPLC since Back to Search Results
Device generator, lesion, radiofrequency
Regulation Description Radiofrequency lesion generator.
Product CodeGXD
Regulation Number 882.4400
Device Class 2


Premarket Reviews
ManufacturerDecision
ABBOTT MEDICAL
  SUBSTANTIALLY EQUIVALENT 1
AVANOS MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
EPIMED INTERNATIONAL
  SUBSTANTIALLY EQUIVALENT 1
NEUROONE MEDICAL TECHNOLOGIES CORP.
  SUBSTANTIALLY EQUIVALENT 1
RF INNOVATIONS, INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2021 154 161
2022 84 84
2023 54 55
2024 63 63
2025 88 88
2026 3 3

Device Problems MDRs with this Device Problem Events in those MDRs
Insufficient Heating 81 81
Fracture 75 75
Output Problem 59 59
Adverse Event Without Identified Device or Use Problem 47 51
Thermal Decomposition of Device 26 26
Communication or Transmission Problem 22 22
Smoking 17 17
Temperature Problem 13 13
Connection Problem 12 12
Unexpected Shutdown 11 11
High impedance 9 9
Overheating of Device 9 9
Failure to Deliver Energy 8 8
Grounding Malfunction 7 7
Mechanical Problem 7 7
Device Emits Odor 6 6
Failure to Power Up 6 6
Impedance Problem 6 6
Degraded 6 6
Unintended Electrical Shock 5 5
Power Problem 5 5
No Display/Image 5 5
Energy Output Problem 4 4
Defective Device 4 4
Insufficient Information 4 4
Patient Device Interaction Problem 3 3
Noise, Audible 3 3
Use of Device Problem 3 3
Structural Problem 3 3
Loss of or Failure to Bond 2 2
Disconnection 2 2
Display or Visual Feedback Problem 2 2
Defibrillation/Stimulation Problem 2 2
No Apparent Adverse Event 2 2
Device Handling Problem 2 2
Low impedance 1 1
Break 1 1
Improper or Incorrect Procedure or Method 1 1
Erratic or Intermittent Display 1 1
Inappropriate/Inadequate Shock/Stimulation 1 1
Fire 1 1
Material Separation 1 1
Failure to Sense 1 1
Operating System Becomes Nonfunctional 1 1
Output below Specifications 1 1
Failure of Device to Self-Test 1 1
Computer Operating System Problem 1 1
Protective Measures Problem 1 1
Application Program Problem 1 1
Patient-Device Incompatibility 1 4

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 370 370
Partial thickness (Second Degree) Burn 25 25
Pain 16 16
Burn(s) 10 11
Full thickness (Third Degree) Burn 9 9
Superficial (First Degree) Burn 7 14
Electric Shock 5 5
Insufficient Information 5 5
Muscle Weakness 4 4
Inadequate Pain Relief 4 4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 3 3
Foreign Body In Patient 3 3
Speech Disorder 2 2
Burning Sensation 2 2
Erythema 2 2
Spinal Cord Injury 2 2
High Blood Pressure/ Hypertension 1 1
Arrhythmia 1 1
Shock from Patient Lead(s) 1 1
Fatigue 1 1
No Information 1 1
Cramp(s) /Muscle Spasm(s) 1 1
Blister 1 1
Paresthesia 1 1
Cellulitis 1 1
Unspecified Nervous System Problem 1 1
Fever 1 1
Osteomyelitis 1 1
Numbness 1 1
Urinary Retention 1 1
Chest Pain 1 1
Nerve Damage 1 1
Peeling 1 1
Fall 1 1
No Consequences Or Impact To Patient 1 1
Constipation 1 1
Bacterial Infection 1 1
Paraplegia 1 1
Ambulation Difficulties 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Abbott II Nov-02-2023
2 Abbott Laboratories Inc. (St Jude Medical) II May-10-2021
3 Avanos Medical, Inc. II Sep-21-2023
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