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TPLC
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Device
unit, neonatal phototherapy
Product Code
LBI
Regulation Number
880.5700
Device Class
2
Premarket Reviews
Manufacturer
Decision
ATOM MEDICAL CORPORATION
SUBSTANTIALLY EQUIVALENT
2
AVALON BIOMEDICAL (SHENZHEN) LIMITED
SUBSTANTIALLY EQUIVALENT
1
BIO-MED USA
SUBSTANTIALLY EQUIVALENT
1
BISTOS CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
DRAEGER MEDICAL SYSTEMS, INC.
SUBSTANTIALLY EQUIVALENT
2
FANEM LDA
SUBSTANTIALLY EQUIVALENT
1
INTERLECTRIC CORP.
SUBSTANTIALLY EQUIVALENT
1
INTERNATIONAL BIOMEDICAL
SUBSTANTIALLY EQUIVALENT
1
LITTLE SPARROWS TECHNOLOGIES, INC.
SUBSTANTIALLY EQUIVALENT
1
LUMITEX, INC.
SUBSTANTIALLY EQUIVALENT
1
MEDIX I.C.S.A.
SUBSTANTIALLY EQUIVALENT
2
NATUS MEDICAL INCORPORATED
SUBSTANTIALLY EQUIVALENT
4
NEOLIGHT, LLC
SUBSTANTIALLY EQUIVALENT
1
NEOMEDLIGHT
SUBSTANTIALLY EQUIVALENT
1
PHYSICIAN ENGINEERED PRODUCTS, INC.
SUBSTANTIALLY EQUIVALENT
2
WIPRO GE HEALTHCARE PRIVATE, LTD.
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2014
5
5
2015
5
5
2016
22
22
2017
577
577
2018
37
37
2019
6
6
2020
6
6
2021
2
2
2022
8
8
2024
4
4
Device Problems
MDRs with this Device Problem
Events in those MDRs
Overheating of Device
416
416
Melted
415
415
Device Issue
79
79
Device Operational Issue
47
47
Low Test Results
45
45
Output Problem
18
18
Use of Device Problem
12
12
Energy Output Problem
12
12
Output below Specifications
11
11
Adverse Event Without Identified Device or Use Problem
8
8
Electrical /Electronic Property Problem
8
8
High Test Results
7
7
Thermal Decomposition of Device
6
6
Device Emits Odor
6
6
Device Operates Differently Than Expected
6
6
Break
5
5
Low Readings
4
4
Detachment of Device or Device Component
4
4
Device Fell
4
4
Smoking
3
3
Appropriate Term/Code Not Available
3
3
Device Dislodged or Dislocated
3
3
Material Twisted/Bent
3
3
Dent in Material
2
2
Failure to Power Up
2
2
Output above Specifications
2
2
Improper or Incorrect Procedure or Method
2
2
Loss of Power
2
2
Temperature Problem
2
2
Failure To Service
2
2
Device Inoperable
2
2
Maintenance Does Not Comply To Manufacturers Recommendations
2
2
Improper Device Output
2
2
Noise, Audible
1
1
No Device Output
1
1
Device Tipped Over
1
1
Excessive Cooling
1
1
Off-Label Use
1
1
Loss of or Failure to Bond
1
1
Patient-Device Incompatibility
1
1
Component Falling
1
1
Component Incompatible
1
1
Unexpected Therapeutic Results
1
1
Nonstandard Device
1
1
Component Missing
1
1
Protective Measures Problem
1
1
Electrical Shorting
1
1
Unexpected Shutdown
1
1
Material Frayed
1
1
Material Protrusion/Extrusion
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
631
631
No Clinical Signs, Symptoms or Conditions
13
13
No Consequences Or Impact To Patient
9
9
Burn(s)
4
5
Skin Irritation
3
3
No Patient Involvement
3
3
No Information
2
2
Burn, Thermal
2
2
Alteration In Body Temperature
2
2
Injury
2
2
Erythema
2
2
Complaint, Ill-Defined
1
1
Skin Inflammation/ Irritation
1
1
Inflammation
1
1
Rash
1
1
Jaundice
1
1
Insufficient Information
1
1
Hemorrhage/Bleeding
1
1
Full thickness (Third Degree) Burn
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Draeger Medical Systems, Inc.
II
Jul-06-2012
2
Lumitex Inc
II
Jan-31-2020
3
Natus Medical Incorporated
II
Apr-14-2017
4
Natus Medical Incorporated
II
Dec-15-2016
5
Natus Medical Incorporated
II
Dec-15-2016
6
Natus Medical Incorporated
II
Jun-15-2016
7
Natus Medical Incorporated
II
Oct-21-2015
8
Natus Medical Incorporated
II
Apr-10-2015
9
Natus Medical Incorporated
II
Dec-22-2014
10
Natus Medical Incorporated
II
Nov-24-2009
11
Ohmeda Medical
II
Mar-20-2017
12
Physician Engineered Products, Inc.
II
Aug-31-2015
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