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TPLC
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Device
plate, bone
Regulation Description
Bone plate.
Product Code
JEY
Regulation Number
872.4760
Device Class
2
Premarket Reviews
Manufacturer
Decision
BIOMET MICROFIXATION
SUBSTANTIALLY EQUIVALENT
1
FAICO MEDICAL LLC
SUBSTANTIALLY EQUIVALENT
1
INDUSTRIAS MEDICAS SAMPEDRO S.A.S.
SUBSTANTIALLY EQUIVALENT
1
INION OY
SUBSTANTIALLY EQUIVALENT
1
KLS-MARTIN L.P.
SUBSTANTIALLY EQUIVALENT
2
MEDCAD
SUBSTANTIALLY EQUIVALENT
2
METICULY CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
MICROWARE PRECISION CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
MONTJADE ENGINEERING CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
REOSS GMBH
SUBSTANTIALLY EQUIVALENT
1
SITES MEDICAL, LLC
SUBSTANTIALLY EQUIVALENT
1
STRYKER
SUBSTANTIALLY EQUIVALENT
2
1. K222650
Stryker Cutomized Mandible Recon Plate; Stryker Su
...
STRYKER CRANIOMAXILLOFACIAL
SUBSTANTIALLY EQUIVALENT
1
1. K222650
Stryker Cutomized Mandible Recon Plate; Stryker Su
...
STRYKER CRANIOMAXILLOFACIAL (CMF)
SUBSTANTIALLY EQUIVALENT
1
1. K222650
Stryker Cutomized Mandible Recon Plate; Stryker Su
...
STRYKER LEIBINGER GMBH & CO. KG
SUBSTANTIALLY EQUIVALENT
3
STRYKER LEIBINGER MICRO IMPLANTS
SUBSTANTIALLY EQUIVALENT
1
SYNTHES (USA) PRODUCTS, LLC
SUBSTANTIALLY EQUIVALENT
1
TECHMAH CMF
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2020
680
680
2021
451
451
2022
344
344
2023
495
495
2024
696
696
2025
826
826
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
1315
1315
Adverse Event Without Identified Device or Use Problem
723
723
Fracture
385
385
Device-Device Incompatibility
171
171
Material Twisted/Bent
156
156
Material Deformation
110
110
Migration
104
104
Device Slipped
103
103
Manufacturing, Packaging or Shipping Problem
88
88
Device Contaminated During Manufacture or Shipping
73
73
Entrapment of Device
64
64
No Apparent Adverse Event
57
57
Crack
48
48
Loosening of Implant Not Related to Bone-Ingrowth
47
47
Difficult to Advance
31
31
Osseointegration Problem
30
30
Device Appears to Trigger Rejection
27
27
Migration or Expulsion of Device
26
26
Failure to Cut
22
22
Defective Device
20
20
Inadequacy of Device Shape and/or Size
18
18
Patient Device Interaction Problem
17
17
Patient-Device Incompatibility
16
16
Material Integrity Problem
16
16
Loss of Osseointegration
15
15
Device Damaged Prior to Use
15
15
Device Dislodged or Dislocated
15
15
Insufficient Information
14
14
Nonstandard Device
12
12
Material Fragmentation
12
12
Noise, Audible
11
11
Packaging Problem
11
11
Use of Device Problem
10
10
Malposition of Device
10
10
Detachment of Device or Device Component
9
9
Material Discolored
8
8
Difficult to Insert
8
8
Failure to Osseointegrate
5
5
Output Problem
5
5
Component Missing
4
4
Positioning Problem
4
4
Device Markings/Labelling Problem
4
4
Improper or Incorrect Procedure or Method
4
4
Dull, Blunt
4
4
Positioning Failure
3
3
Difficult or Delayed Positioning
3
3
Tear, Rip or Hole in Device Packaging
3
3
Appropriate Term/Code Not Available
3
3
Naturally Worn
3
3
Mechanical Jam
3
3
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
1715
1715
Unspecified Infection
252
252
No Consequences Or Impact To Patient
246
246
Insufficient Information
205
205
Failure of Implant
151
151
Pain
149
149
Non-union Bone Fracture
138
138
Foreign Body In Patient
127
127
No Code Available
120
120
Impaired Healing
85
85
Swelling/ Edema
75
75
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
73
73
Unspecified Tissue Injury
70
70
No Known Impact Or Consequence To Patient
64
64
Physical Asymmetry
38
38
Wound Dehiscence
32
32
Nerve Damage
32
32
Discomfort
29
29
No Patient Involvement
28
28
Inflammation
27
27
No Information
26
26
Inadequate Osseointegration
24
24
Post Operative Wound Infection
24
24
Difficulty Chewing
23
23
Bacterial Infection
23
23
Confusion/ Disorientation
21
21
Hypersensitivity/Allergic reaction
18
18
Purulent Discharge
16
16
Bone Fracture(s)
15
15
Headache
14
14
Cerebrospinal Fluid Leakage
14
14
Loss of Range of Motion
14
14
Erythema
14
14
Skin Inflammation/ Irritation
14
14
Inadequate Pain Relief
13
13
Swelling
13
13
Implant Pain
12
12
Limited Mobility Of The Implanted Joint
12
12
Obstruction/Occlusion
11
11
Paralysis
11
11
Necrosis
10
10
Paresthesia
10
10
Fluid Discharge
8
8
Device Embedded In Tissue or Plaque
8
8
Foreign Body Reaction
8
8
Visual Disturbances
8
8
Malunion of Bone
7
7
Fistula
7
7
Deformity/ Disfigurement
6
6
Difficulty Chewing
6
6
Recalls
Manufacturer
Recall Class
Date Posted
1
Biomet, Inc.
II
Dec-17-2020
2
Materialise N.V.
II
Aug-03-2023
3
Materialise N.V.
II
Apr-06-2020
4
Synthes Produktions GmbH
II
Jul-30-2020
5
Synthes, Inc.
II
Jul-24-2020
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