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TPLC
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Device
hearing aid, bone conduction, implanted
Product Code
MAH
Regulation Number
874.3302
Device Class
2
Premarket Reviews
Manufacturer
Decision
COCHLEAR AMERICAS
SUBSTANTIALLY EQUIVALENT
3
OTICON MEDICAL AB
SUBSTANTIALLY EQUIVALENT
6
MDR Year
MDR Reports
MDR Events
2014
46
46
2015
52
52
2016
308
308
2017
614
614
2018
629
629
2019
635
635
2020
692
692
2021
709
709
2022
712
712
2023
746
746
2024
257
257
Device Problems
MDRs with this Device Problem
Events in those MDRs
Appropriate Term/Code Not Available
2347
2347
Patient Device Interaction Problem
1033
1033
Loss of Osseointegration
763
763
Adverse Event Without Identified Device or Use Problem
541
541
Failure to Osseointegrate
540
540
Insufficient Information
109
109
Loosening of Implant Not Related to Bone-Ingrowth
57
57
Osseointegration Problem
36
36
Inadequacy of Device Shape and/or Size
17
17
Extrusion
16
16
No Apparent Adverse Event
14
14
Detachment of Device or Device Component
12
12
Patient-Device Incompatibility
12
12
Biocompatibility
8
8
Device Appears to Trigger Rejection
5
5
Device Displays Incorrect Message
3
3
Device Operates Differently Than Expected
3
3
Device Dislodged or Dislocated
2
2
Expulsion
2
2
Connection Problem
2
2
Failure to Deliver Shock/Stimulation
2
2
Explanted
2
2
Fracture
2
2
Signal Artifact/Noise
2
2
Thermal Decomposition of Device
2
2
Mechanical Problem
2
2
Product Quality Problem
2
2
Use of Device Problem
2
2
Therapeutic or Diagnostic Output Failure
2
2
Output Problem
1
1
Migration
1
1
Contamination
1
1
High impedance
1
1
Device remains implanted
1
1
Shelf Life Exceeded
1
1
Device Slipped
1
1
Unexpected Therapeutic Results
1
1
Improper or Incorrect Procedure or Method
1
1
Microbial Contamination of Device
1
1
Component Missing
1
1
Malposition of Device
1
1
Implant breakage or physical damage
1
1
Expiration Date Error
1
1
Separation Failure
1
1
Defective Device
1
1
Device Operational Issue
1
1
Human-Device Interface Problem
1
1
Compatibility Problem
1
1
No Flow
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Unspecified Infection
999
999
Inadequate Osseointegration
798
798
Skin Infection
609
609
No Code Available
531
531
Impaired Healing
507
507
Bacterial Infection
411
411
Host-Tissue Reaction
401
401
Pain
325
325
Patient Problem/Medical Problem
309
309
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
237
237
Head Injury
151
151
Skin Inflammation/ Irritation
133
133
No Clinical Signs, Symptoms or Conditions
117
117
Cellulitis
91
91
Inflammation
86
86
Fluid Discharge
80
80
Insufficient Information
70
70
Scar Tissue
62
62
Skin Irritation
58
58
Swelling/ Edema
58
58
Swelling
55
55
Purulent Discharge
52
52
Post Operative Wound Infection
50
50
Hearing Impairment
48
48
No Information
44
44
Discomfort
26
26
Erythema
25
25
Implant Pain
24
24
Foreign Body Reaction
22
22
Wound Dehiscence
22
22
Discharge
21
21
Skin Inflammation
21
21
Tissue Breakdown
20
20
Staphylococcus Aureus
19
19
Abscess
16
16
Irritation
14
14
Skin Disorders
13
13
Hemorrhage/Bleeding
12
12
Failure of Implant
11
11
Headache
11
11
Drug Resistant Bacterial Infection
11
11
Injury
10
10
No Consequences Or Impact To Patient
10
10
Fall
7
7
Granuloma
6
6
Meningitis
6
6
Necrosis Of Flap Tissue
5
5
Necrosis
4
4
Hematoma
4
4
Deafness
4
4
Skin Burning Sensation
4
4
No Known Impact Or Consequence To Patient
3
3
Skin Erosion
3
3
Erosion
3
3
Hypersensitivity/Allergic reaction
3
3
Nausea
2
2
Edema
2
2
Burning Sensation
2
2
Ulcer
2
2
Post Traumatic Wound Infection
2
2
No Patient Involvement
2
2
Missing Value Reason
2
2
Reaction to Medicinal Component of Device
2
2
Osteomyelitis
1
1
Inadequate Pain Relief
1
1
Dizziness
1
1
Scarring
1
1
Atrial Fibrillation
1
1
Undesired Nerve Stimulation
1
1
Rash
1
1
Intracranial Hemorrhage
1
1
Itching Sensation
1
1
Infiltration into Tissue
1
1
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