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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device clamp, vascular
Regulation Description Vascular clamp.
Product CodeDXC
Regulation Number 870.4450
Device Class 2


Premarket Reviews
ManufacturerDecision
BEIJING DEMAX MEDICAL TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
BIOREP TECHNOLOGIES, INC
  SUBSTANTIALLY EQUIVALENT 1
CAREFUSION 2200 INC
  SUBSTANTIALLY EQUIVALENT 1
COMPRESSION WORKS INC
  SUBSTANTIALLY EQUIVALENT 1
ENSITE VACULAR, LLC
  SUBSTANTIALLY EQUIVALENT 1
ENSITE VASCULAR
  SUBSTANTIALLY EQUIVALENT 2
KONO SEISAKUSHO CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
MEDICAL INGENUITIES
  SUBSTANTIALLY EQUIVALENT 1
NINGBO DIZEGENS MEDICAL SCIENCE CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
  1.  K232577  Radial Compression Device
SUNNY MEDICAL DEVICE (SHENZHEN) CO.,LTD.
  SUBSTANTIALLY EQUIVALENT 1
SYNOVIS MICRO COMPANIES ALLIANCE, INC.
  SUBSTANTIALLY EQUIVALENT 1
TERUMO MEDICAL CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
VASCULAR GRAFT SOLUTIONS, LTD.
  SUBSTANTIALLY EQUIVALENT 2
VASOINNOVATIONS INC.
  SUBSTANTIALLY EQUIVALENT 1
VASOINNOVATIONS, INC
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2019 393 393
2020 404 404
2021 371 371
2022 273 273
2023 674 674
2024 375 375
2025 23 23

Device Problems MDRs with this Device Problem Events in those MDRs
Fitting Problem 679 679
Activation Problem 351 351
Gas/Air Leak 306 306
Deflation Problem 234 234
Failure to Unfold or Unwrap 159 159
Break 97 97
Difficult to Open or Close 97 97
Adverse Event Without Identified Device or Use Problem 91 91
Leak/Splash 69 69
Insufficient Information 64 64
Crack 61 61
Inflation Problem 46 46
Unraveled Material 36 36
Activation, Positioning or Separation Problem 36 36
Mechanical Problem 34 34
Material Rupture 32 32
Unintended Deflation 31 31
Detachment of Device or Device Component 30 30
No Apparent Adverse Event 30 30
Premature Activation 24 24
Appropriate Term/Code Not Available 24 24
Material Puncture/Hole 23 23
Failure to Seal 19 19
Burst Container or Vessel 16 16
Material Twisted/Bent 15 15
Material Separation 15 15
Fluid/Blood Leak 13 13
Filling Problem 11 11
Use of Device Problem 10 10
Unintended Movement 9 9
Device Slipped 9 9
Migration 9 9
Defective Device 9 9
Decrease in Pressure 8 8
Failure to Cut 8 8
Difficult to Insert 7 7
Device Contamination with Chemical or Other Material 6 6
Therapeutic or Diagnostic Output Failure 6 6
Manufacturing, Packaging or Shipping Problem 6 6
Component Missing 6 6
Delivered as Unsterile Product 6 6
Physical Resistance/Sticking 5 5
Device Dislodged or Dislocated 5 5
Material Deformation 5 5
Misfire 5 5
Failure to Fire 5 5
Material Split, Cut or Torn 4 4
Patient Device Interaction Problem 4 4
Loose or Intermittent Connection 4 4
Failure to Advance 4 4

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 1344 1344
No Consequences Or Impact To Patient 553 553
Hematoma 165 165
Hemorrhage/Bleeding 156 156
No Known Impact Or Consequence To Patient 103 103
Insufficient Information 97 97
Blood Loss 69 69
No Patient Involvement 59 59
Pain 16 16
Injury 12 12
No Information 10 10
Bruise/Contusion 10 10
Death 9 9
Foreign Body In Patient 8 8
Pseudoaneurysm 7 7
Swelling/ Edema 6 6
Laceration(s) 5 5
Numbness 5 5
Nerve Damage 4 4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 4 4
Unspecified Infection 4 4
Vascular Dissection 3 3
No Code Available 3 3
Thrombosis/Thrombus 3 3
Cyanosis 3 3
Cardiac Arrest 3 3
Perforation of Vessels 3 3
Ventricular Fibrillation 3 3
Necrosis 3 3
Unspecified Heart Problem 2 2
Failure of Implant 2 2
Cardiovascular Insufficiency 2 2
Rupture 2 2
Diminished Pulse Pressure 2 2
Nervous System Injury 2 2
Heart Failure/Congestive Heart Failure 1 1
Embolism/Embolus 1 1
Multiple Organ Failure 1 1
Discomfort 1 1
Loss of consciousness 1 1
Obstruction/Occlusion 1 1
Needle Stick/Puncture 1 1
Pallor 1 1
Aortic Dissection 1 1
Skin Tears 1 1
Device Embedded In Tissue or Plaque 1 1
Burn, Thermal 1 1
Patient Problem/Medical Problem 1 1
Tissue Breakdown 1 1
Ascites 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Baxter Healthcare Corporation II Apr-12-2024
2 Baxter Healthcare Corporation II Jan-05-2024
3 Baxter Healthcare Corporation II Apr-29-2022
4 Edwards Lifesciences, LLC I Jun-11-2019
5 Edwards Lifesciences, LLC II Apr-06-2019
6 Integra LifeSciences Corp. II Aug-30-2019
7 Merit Medical Systems, Inc. II Apr-24-2020
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