• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search show TPLC since Back to Search Results
Device endoscopic grasping/cutting instrument, non-powered
Regulation Description Endoscope and accessories.
Definition To manually grasp stones, tissues or other objects through an endoscope. To manipulate, sample or cut tissues through an endoscope.
Product CodeOCZ
Regulation Number 876.1500
Device Class 2


Premarket Reviews
ManufacturerDecision
ENVISION ENDOSCOPY
  SUBSTANTIALLY EQUIVALENT 1
ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 21 21
2021 20 20
2022 33 33
2023 25 25
2024 37 37
2025 22 22

Device Problems MDRs with this Device Problem Events in those MDRs
Break 53 53
Difficult to Open or Close 22 22
Adverse Event Without Identified Device or Use Problem 14 14
Material Fragmentation 11 11
Material Separation 9 9
Detachment of Device or Device Component 9 9
Insufficient Information 7 7
Mechanical Problem 6 6
Arcing 4 4
Difficult to Remove 4 4
Improper or Incorrect Procedure or Method 3 3
Flushing Problem 3 3
Material Twisted/Bent 3 3
Mechanical Jam 3 3
Mechanics Altered 3 3
Temperature Problem 3 3
Use of Device Problem 2 2
Entrapment of Device 2 2
Unintended Movement 2 2
Physical Resistance/Sticking 2 2
Failure to Cut 2 2
Defective Device 2 2
Activation, Positioning or Separation Problem 2 2
Arcing of Electrodes 1 1
Tear, Rip or Hole in Device Packaging 1 1
Device Reprocessing Problem 1 1
Material Deformation 1 1
Material Integrity Problem 1 1
Packaging Problem 1 1
Activation Failure 1 1
Sharp Edges 1 1
Device Fell 1 1
Unexpected Shutdown 1 1
Activation Problem 1 1
Connection Problem 1 1
Device Damaged by Another Device 1 1
Electrical Overstress 1 1
Unsealed Device Packaging 1 1
Product Quality Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 85 85
Insufficient Information 30 30
Foreign Body In Patient 15 15
No Code Available 5 5
No Consequences Or Impact To Patient 5 5
Superficial (First Degree) Burn 4 4
No Known Impact Or Consequence To Patient 4 4
Laceration(s) 4 4
Burn(s) 3 3
Hemorrhage/Bleeding 3 3
Perforation 2 2
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Abdominal Distention 1 1
No Patient Involvement 1 1
Bowel Perforation 1 1
Patient Problem/Medical Problem 1 1
Partial thickness (Second Degree) Burn 1 1
Device Embedded In Tissue or Plaque 1 1
Pericardial Effusion 1 1
Unspecified Kidney or Urinary Problem 1 1
Pain 1 1
Tissue Damage 1 1
Abdominal Pain 1 1
Death 1 1
Granuloma 1 1
Low Blood Pressure/ Hypotension 1 1
Blister 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Hobbs Medical, Inc. II Oct-07-2022
2 Hobbs Medical, Inc. II Jul-15-2022
3 Shent USA, Inc. II Aug-06-2021
-
-