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TPLC
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Device
confocal optical imaging
Regulation Description
Endoscope and accessories.
Definition
Collection of light signals for visualization of cellular microstructures.
Product Code
OWN
Regulation Number
876.1500
Device Class
2
Premarket Reviews
Manufacturer
Decision
ACTIV SURGICAL, INC.
SUBSTANTIALLY EQUIVALENT
2
GUANGDONG OPTOMEDIC TECHNOLOGIES, INC.
SUBSTANTIALLY EQUIVALENT
1
KARL STORZ ENDOSCOPY AMERICA
SUBSTANTIALLY EQUIVALENT
1
KARL STORZ ENDOSCOPY_AMERICA, INC.
SUBSTANTIALLY EQUIVALENT
1
KARL STORZ SE & CO.KG
SUBSTANTIALLY EQUIVALENT
2
KARL STORZ-ENDOSCOPY-AMERICA, INC.
SUBSTANTIALLY EQUIVALENT
1
MAUNA KEA TECHNOLOGIES
SUBSTANTIALLY EQUIVALENT
4
NOVADAQ TECHNOLOGIES ULC. (NOW A PART OF STRYKER)
SUBSTANTIALLY EQUIVALENT
2
OLYMPUS MEDICAL SYSTEMS CORP.
SUBSTANTIALLY EQUIVALENT
2
OPTOSURGICAL, LLC
SUBSTANTIALLY EQUIVALENT
1
SAMANTREE MEDICAL SA
SUBSTANTIALLY EQUIVALENT
1
SMARTSURGN INCORPORATED
SUBSTANTIALLY EQUIVALENT
1
STRYKER
SUBSTANTIALLY EQUIVALENT
3
VISIONSENSE, LTD.
SUBSTANTIALLY EQUIVALENT
2
WUXI HISKY MEDICAL TECHNOLOGIES CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2020
105
105
2021
312
313
2022
346
346
2023
164
164
2024
165
165
2025
177
177
Device Problems
MDRs with this Device Problem
Events in those MDRs
No Display/Image
352
352
Output Problem
270
270
Communication or Transmission Problem
120
120
Temperature Problem
113
113
Optical Problem
104
104
Poor Quality Image
98
98
Electrical /Electronic Property Problem
80
80
Failure to Power Up
46
46
Display or Visual Feedback Problem
36
37
Erratic or Intermittent Display
35
35
Overheating of Device
30
30
Energy Output Problem
22
22
Thermal Decomposition of Device
21
21
Adverse Event Without Identified Device or Use Problem
21
21
Break
19
19
Fogging
18
18
Insufficient Information
16
16
No Device Output
16
16
Power Problem
13
13
Electrical Power Problem
13
13
Material Integrity Problem
12
12
Excessive Heating
11
11
Image Display Error/Artifact
11
11
Connection Problem
11
11
Electrical Overstress
11
11
Use of Device Problem
11
11
Device Sensing Problem
10
10
Failure to Shut Off
10
10
Defective Component
10
10
Optical Distortion
10
10
Smoking
9
9
Intermittent Loss of Power
9
9
Activation Failure
8
8
Unexpected Shutdown
8
8
Optical Obstruction
6
6
Loss of Power
6
6
Computer Software Problem
5
5
Component Misassembled
5
5
Detachment of Device or Device Component
5
5
Environmental Compatibility Problem
5
5
Moisture or Humidity Problem
5
5
Circuit Failure
5
5
Therapeutic or Diagnostic Output Failure
5
5
Contamination /Decontamination Problem
4
4
Material Twisted/Bent
4
4
Defective Device
4
4
Misfocusing
4
4
Electro-Static Discharge
4
4
Loose or Intermittent Connection
4
4
Mechanical Problem
4
4
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
1092
1092
Insufficient Information
164
165
No Consequences Or Impact To Patient
73
73
No Known Impact Or Consequence To Patient
42
42
Burn(s)
39
39
Superficial (First Degree) Burn
14
14
Electric Shock
6
6
No Patient Involvement
6
6
Burn, Thermal
3
3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
2
2
Bowel Perforation
2
2
Abrasion
2
2
Syncope/Fainting
1
1
Necrosis
1
1
Laceration(s)
1
1
Shock
1
1
Unspecified Tissue Injury
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Olympus Corporation of the Americas
II
Oct-25-2024
2
Visionsense, Ltd.
II
Nov-23-2022
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