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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device indicator, biological sterilization process
Product CodeFRC
Regulation Number 880.2800
Device Class 2


Premarket Reviews
ManufacturerDecision
3M
  SUBSTANTIALLY EQUIVALENT 1
3M COMPANY
  SUBSTANTIALLY EQUIVALENT 24
3M COMPANY-3M HEALTH CARE
  SUBSTANTIALLY EQUIVALENT 1
3M COMPLANY
  SUBSTANTIALLY EQUIVALENT 1
ADVANCED STERILIZATION PRODUCTS
  SUBSTANTIALLY EQUIVALENT 9
ADVANCED STERILIZATION PRODUCTS (ASP)
  SUBSTANTIALLY EQUIVALENT 3
ANDERSEN STERILIZERS, INC.
  SUBSTANTIALLY EQUIVALENT 4
ANDERSEN STERILIZERS,INC.
  SUBSTANTIALLY EQUIVALENT 1
BCR DIAGNOSTICS, INC.
  SUBSTANTIALLY EQUIVALENT 1
CROSSTEX INTERNATIONAL
  SUBSTANTIALLY EQUIVALENT 1
CROSSTEX/SPSMEDICAL, A DIVISION OF CANTEL MEDICAL
  SUBSTANTIALLY EQUIVALENT 2
DANA PRODUCTS, INC.
  SUBSTANTIALLY EQUIVALENT 3
GKE-GMBH
  SUBSTANTIALLY EQUIVALENT 1
MESA LABORATORIES, INC.
  SUBSTANTIALLY EQUIVALENT 3
NORTH AMERICAN SCIENCE ASSOC., INC.
  SUBSTANTIALLY EQUIVALENT 3
PLASMAPP CO,.LTD.
  SUBSTANTIALLY EQUIVALENT 1
PLASMAPP CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
RAVEN BIOLOGICAL LABORATORIES, INC.
  SUBSTANTIALLY EQUIVALENT 1
SGM BIOTECH, INC.
  SUBSTANTIALLY EQUIVALENT 2
SPS MEDICAL SUPPLY CORP.
  SUBSTANTIALLY EQUIVALENT 2
SPSMEDICAL SUPPLY CORP. A DIVISION OF CANTEL MEDICAL
  SUBSTANTIALLY EQUIVALENT 1
STERILUCENT, INC
  SUBSTANTIALLY EQUIVALENT 2
STERILUCENT, INC.
  SUBSTANTIALLY EQUIVALENT 1
STERIS
  SUBSTANTIALLY EQUIVALENT 1
STERIS CORPORATION
  SUBSTANTIALLY EQUIVALENT 28
STERIS CORPORATIONS
  SUBSTANTIALLY EQUIVALENT 3
STERITEC PRODUCTS MFG. CO., INC.
  SUBSTANTIALLY EQUIVALENT 1
STERITEC PRODUCTS MFG., CO., INC.
  SUBSTANTIALLY EQUIVALENT 2
TERRAGENE SA
  SUBSTANTIALLY EQUIVALENT 3
TRUE INDICATING LLC
  SUBSTANTIALLY EQUIVALENT 1
TSO3 INC.
  SUBSTANTIALLY EQUIVALENT 1
TSO3 INC., NOW A PART OF STRYKER
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2014 51 51
2015 182 182
2016 479 479
2017 182 182
2018 22 22
2019 30 30
2020 16 16
2021 10 10
2022 9 9
2023 20 20
2024 20 20

Device Problems MDRs with this Device Problem Events in those MDRs
Appropriate Term/Code Not Available 639 639
Chemical Problem 291 291
Device Operates Differently Than Expected 172 172
Improper or Incorrect Procedure or Method 9 9
Leak/Splash 7 7
Environmental Particulates 7 7
Insufficient Information 7 7
Adverse Event Without Identified Device or Use Problem 7 7
False Positive Result 6 6
Shelf Life Exceeded 5 5
Break 4 4
Incorrect, Inadequate or Imprecise Result or Readings 4 4
Use of Device Problem 4 4
Contamination /Decontamination Problem 3 3
Contamination of Device Ingredient or Reagent 3 3
Device Contamination With Biological Material 3 3
Component Missing 3 3
Fluid/Blood Leak 2 2
Device Disinfection Or Sterilization Issue 2 2
Problem with Sterilization 2 2
Incorrect Or Inadequate Test Results 2 2
Material Fragmentation 2 2
Defective Device 2 2
Output Problem 2 2
Chemical Spillage 1 1
Manufacturing, Packaging or Shipping Problem 1 1
Therapeutic or Diagnostic Output Failure 1 1
Device Expiration Issue 1 1
Improper Chemical Reaction 1 1
Poor Quality Image 1 1
No Apparent Adverse Event 1 1
Material Separation 1 1
Device Damaged Prior to Use 1 1
Device Operational Issue 1 1
Off-Label Use 1 1
Microbial Contamination of Device 1 1
Material Rupture 1 1
Packaging Problem 1 1
Sterility 1 1
Failure of Device to Self-Test 1 1
Device Reprocessing Problem 1 1
False Negative Result 1 1
Device Contaminated During Manufacture or Shipping 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Patient Involvement 466 466
No Known Impact Or Consequence To Patient 461 461
No Clinical Signs, Symptoms or Conditions 48 48
No Consequences Or Impact To Patient 41 41
No Information 17 17
No Code Available 6 6
Burn(s) 4 4
Test Result 3 3
Chemical Exposure 2 2
Insufficient Information 2 2
Laceration(s) 2 2
Patient Problem/Medical Problem 1 1
Respiratory Distress 1 1
Skin Irritation 1 1
Abrasion 1 1
Skin Discoloration 1 1
Fever 1 1
Injury 1 1
Discomfort 1 1
Eye Injury 1 1
Caustic/Chemical Burns 1 1
Bacterial Infection 1 1
Infiltration into Tissue 1 1
Eye Pain 1 1
Premature Labor 1 1

Recalls
Manufacturer Recall Class Date Posted
1 3M Company - Health Care Business II Sep-26-2023
2 3M Company - Health Care Business II Jul-07-2014
3 Advanced Sterilization Products II Dec-28-2013
4 Advanced Sterilization Products II Apr-26-2013
5 Advanced Sterilization Products II Dec-12-2012
6 Advanced Sterilization Products II Jul-27-2012
7 Advanced Sterilization Products II Jun-06-2012
8 Advanced Sterilization Products II Oct-20-2009
9 Getinge USA Inc II Aug-21-2013
10 Mckesson Medical-Surgical Inc. Corporate Office III Sep-26-2022
11 Mesa Laboratories Bozeman Manufacturing Facility II Mar-29-2018
12 Mesa Laboratories Inc II Jan-26-2017
13 Mesa Laboratories, Inc., Bozeman Manufacturing Facility II Aug-01-2013
14 Steris Corporation II Jan-03-2023
15 Steris Corporation II Dec-28-2013
16 Steritec Products Mfc. Co., Inc. II Jul-29-2013
17 TERRAGENE S.A. II Jan-26-2024
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