• 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 photocoagulator and accessories
Product CodeHQB
Regulation Number 886.4690
Device Class 2


Premarket Reviews
ManufacturerDecision
VITREQ B.V.
  SUBSTANTIALLY EQUIVALENT 1
VORTEX SURGICAL INC
  SUBSTANTIALLY EQUIVALENT 1
VORTEX SURGICAL INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2018 3 3
2019 1 1
2020 14 14
2021 1 1
2022 3 3

Device Problems MDRs with this Device Problem Events in those MDRs
Firing Problem 4 4
Failure to Deliver Energy 3 3
Device Operational Issue 3 3
Gas/Air Leak 3 3
Insufficient Information 2 2
Appropriate Term/Code Not Available 2 2
Mechanical Problem 2 2
Fitting Problem 1 1
Incomplete or Missing Packaging 1 1
Defective Device 1 1
Detachment of Device or Device Component 1 1
Ejection Problem 1 1
Unintended Ejection 1 1
Loose or Intermittent Connection 1 1
Break 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Consequences Or Impact To Patient 10 10
Pain 4 4
No Clinical Signs, Symptoms or Conditions 3 3
No Code Available 3 3
Awareness during Anaesthesia 2 2
No Known Impact Or Consequence To Patient 2 2
Radiation Exposure, Unintended 2 2
Eye Injury 1 1
Conjunctivitis 1 1

-
-