Quick Links: Skip to main page content
Skip to Search
Skip to Topics Menu
Skip to Common Links
U.S. Food & Drug Administration
Follow FDA
En Español
Search FDA
Home
Food
Drugs
Medical Devices
Radiation-Emitting Products
Vaccines, Blood & Biologics
Animal & Veterinary
Cosmetics
Tobacco Products
TPLC - Total Product Life Cycle
FDA Home
medical devices
databases
-
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
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
Back to Search Results
Device
sling, overhead suspension, wheelchair
Product Code
INE
Regulation Number
890.3910
Device Class
1
MDR Year
MDR Reports
MDR Events
2014
2
2
2015
9
9
2016
6
6
2017
1
1
2021
1
1
Device Problems
MDRs with this Device Problem
Events in those MDRs
Material Frayed
5
5
Break
4
4
Torn Material
2
2
Material Separation
2
2
Material Split, Cut or Torn
1
1
Crack
1
1
Degraded
1
1
Unraveled Material
1
1
Use of Device Problem
1
1
Adverse Event Without Identified Device or Use Problem
1
1
Tear, Rip or Hole in Device Packaging
1
1
Detachment of Device or Device Component
1
1
Fracture
1
1
Device Operates Differently Than Expected
1
1
Improper or Incorrect Procedure or Method
1
1
Component Falling
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
9
9
Death
2
2
Laceration(s)
2
2
No Consequences Or Impact To Patient
2
2
No Clinical Signs, Symptoms or Conditions
1
1
No Information
1
1
Head Injury
1
1
Contusion
1
1
Fall
1
1
-
-