Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 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
Use of Device Problem 4 4
Incorrect, Inadequate or Imprecise Result or Readings 4 4
Device Contamination With Biological Material 3 3
Contamination of Device Ingredient or Reagent 3 3
Component Missing 3 3
Contamination /Decontamination Problem 3 3
Material Fragmentation 2 2
Incorrect Or Inadequate Test Results 2 2
Problem with Sterilization 2 2
Defective Device 2 2
Device Disinfection Or Sterilization Issue 2 2
Output Problem 2 2
Fluid/Blood Leak 2 2
Microbial Contamination of Device 1 1
Therapeutic or Diagnostic Output Failure 1 1
Manufacturing, Packaging or Shipping Problem 1 1
Device Expiration Issue 1 1
Chemical Spillage 1 1
Material Rupture 1 1
Packaging Problem 1 1
Device Damaged Prior to Use 1 1
Poor Quality Image 1 1
Material Separation 1 1
No Apparent Adverse Event 1 1
Device Operational Issue 1 1
Off-Label Use 1 1
False Negative Result 1 1
Device Reprocessing Problem 1 1
Sterility 1 1
Failure of Device to Self-Test 1 1
Improper Chemical Reaction 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
Injury 1 1
Fever 1 1
Discomfort 1 1
Eye Injury 1 1
Caustic/Chemical Burns 1 1
Infiltration into Tissue 1 1
Bacterial Infection 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
-
-