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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device device, monitoring, intracranial pressure
Regulation Description Intracranial pressure monitoring device.
Product CodeGWM
Regulation Number 882.1620
Device Class 2


Premarket Reviews
ManufacturerDecision
BRAINCARE DESENVOLVIMENTO E INOVACAO TECNOLOGICA S.A.
  SUBSTANTIALLY EQUIVALENT 1
BRAINCARE DESENVOLVIMENTO E INOVAÇÃO TECNOLÓGICA S.A.
  SUBSTANTIALLY EQUIVALENT 1
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
  SUBSTANTIALLY EQUIVALENT 2
MEDTRONIC, INC.
  SUBSTANTIALLY EQUIVALENT 3
RAUMEDIC AG
  SUBSTANTIALLY EQUIVALENT 1
SOPHYSA
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 268 268
2021 211 211
2022 424 425
2023 744 744
2024 641 641
2025 446 446
2026 151 151

Device Problems MDRs with this Device Problem Events in those MDRs
Fluid/Blood Leak 907 907
Break 398 399
Fracture 360 361
Disconnection 312 312
Incorrect, Inadequate or Imprecise Result or Readings 310 310
Output Problem 154 154
Incorrect Measurement 103 103
Electrical /Electronic Property Problem 69 69
Infusion or Flow Problem 68 68
Unexpected Shutdown 61 61
Insufficient Device Problem Information 59 59
No Device Output 47 47
Complete Blockage 42 42
Device Dislodged or Dislocated 42 42
Display or Visual Feedback Problem 39 39
Device Sensing Problem 37 37
Failure to Read Input Signal 36 36
Adverse Event Without Identified Device or Use Problem 35 35
Loose or Intermittent Connection 34 34
Failure to Zero 34 34
Leak/Splash 32 32
Low Readings 27 27
Connection Problem 27 27
High Readings 25 25
Signal Artifact/Noise 17 17
Unable to Obtain Readings 14 14
Audible Prompt/Feedback Problem 13 13
Imprecise or Erratic Results 12 12
Mechanical Problem 11 11
Appropriate Device Problem Term/Code Not Available 11 11
Device-Device Incompatibility 10 10
Loss of or Failure to Bond 10 10
Image Display Error/Artifact 9 9
Mechanical Jam 9 9
Device Displays Incorrect Message 9 9
Use of Device Problem 8 8
Nonstandard Device 8 8
Pressure Problem 8 8
Material Split, Cut or Torn 8 8
Material Integrity Problem 6 6
Unstable 5 5
Communication or Transmission Problem 5 5
Stretched 4 4
Improper or Incorrect Procedure or Method 4 4
Failure to Transmit Record 4 4
Component Missing 4 4
Obstruction of Flow 4 4
Failure to Calibrate 4 4
Crack 4 4
Deformation Due to Compressive Stress 3 3

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 2045 2046
Insufficient Information 331 331
No Known Impact Or Consequence To Patient 165 165
Cerebrospinal Fluid Leakage 73 73
Injury 52 52
Unspecified Infection 40 40
Failure of Implant 39 39
No Consequences Or Impact To Patient 36 36
Unspecified Tissue Injury 21 21
Bacterial Infection 15 15
Foreign Body In Patient 12 12
Headache 12 12
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available 12 12
Device Embedded In Tissue or Plaque 10 10
Fever 9 9
Hematoma 8 8
Intracranial Hemorrhage 7 7
Hemorrhage/Blood Loss/Bleeding 4 4
Cerebral Edema 4 4
Not Applicable 4 4
Intracranial Pressure Increased 4 4
Pneumocephalus 3 3
Malaise 3 3
Ambulation or Postural Difficulties 3 3
Coma 3 3
Vomiting 3 3
Hydrocephalus 3 3
Death 3 3
Brain Injury 3 3
Unspecified Nervous System Problem 2 2
No Patient Involvement 2 2
Visual Disturbances 2 2
Convulsion/Seizure 2 2
Swelling/ Edema 2 2
Muscle Weakness/Atrophy 2 2
Pain 2 2
Meningitis 2 2
No Code Available 2 2
Loss of consciousness 1 1
Exposure to Body Fluids 1 1
Hernia 1 1
Abrasion 1 1
Skin Inflammation/ Irritation 1 1
Cough 1 1
Hemorrhage, Subarachnoid 1 1
Irritability 1 1
Respiratory Failure 1 1
Seizures 1 1
Cognitive Changes 1 1
Confusion/ Disorientation 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Integra LifeSciences Corp. I Dec-14-2023
2 Integra LifeSciences Corp. II May-19-2023
3 Integra LifeSciences Corp. I Jul-22-2022
4 Integra LifeSciences Corp. (NeuroSciences) II Jan-08-2026
5 Medtronic Neurosurgery I Dec-19-2024
6 Smiths Medical ASD, Inc. II Oct-23-2024
7 Sophysa II Jan-08-2026
8 Sophysa S.A. II May-15-2024
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