• 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 dilator, lachrymal
Product CodeHNW
Regulation Number 886.4350
Device Class 1

MDR Year MDR Reports MDR Events
2014 1 1
2015 1 1
2020 3 3
2023 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
Break 4 4
Detachment Of Device Component 1 1
Material Fragmentation 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 3 3
Dry Eye(s) 2 2
No Consequences Or Impact To Patient 1 1
No Known Impact Or Consequence To Patient 1 1

-
-