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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Super Search Devices@FDA
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New Search show TPLC since Back to Search Results
Device device, analysis, anterior segment
Product CodeMXK
Regulation Number 886.1850
Device Class 2


Premarket Reviews
ManufacturerDecision
C.S.O. S.R.L.
  SUBSTANTIALLY EQUIVALENT 1
OCULUS OPTIKGERATE GMBH
  SUBSTANTIALLY EQUIVALENT 1
OCULUS OPTIKGERÄTE GMBH
  SUBSTANTIALLY EQUIVALENT 1
SANTEC CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
SIS AG, SURGICAL INSTRUMENT SYSTEMS
  SUBSTANTIALLY EQUIVALENT 1
VISIA IMAGING S.R.L.
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2019 2 2
2020 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
Incorrect, Inadequate or Imprecise Result or Readings 2 2
Appropriate Term/Code Not Available 1 1
Incorrect Measurement 1 1

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

Recalls
Manufacturer Recall Class Date Posted
1 Oculus Optikgeraete GMBH II Aug-30-2023
2 Oculus Optikgeraete GMBH II Sep-02-2022
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