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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device handpiece, rotary bone cutting
Regulation Description Bone cutting instrument and accessories.
Product CodeKMW
Regulation Number 872.4120
Device Class 2


Premarket Reviews
ManufacturerDecision
NAKANISHI, INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 13 13
2021 32 32
2022 54 54
2023 25 25
2024 49 49
2025 24 24
2026 23 23

Device Problems MDRs with this Device Problem Events in those MDRs
Overheating of Device 148 148
Temperature Problem 15 15
Power Problem 11 11
Detachment of Device or Device Component 7 7
Break 3 3
Unintended Power Up 2 2
Material Fragmentation 2 2
Mechanical Problem 1 1
Unintended Electrical Shock 1 1
Failure to Power Up 1 1
Use of Device Problem 1 1
Insufficient Device Problem Information 1 1
Fracture 1 1
Intermittent Loss of Power 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Burn(s) 103 103
Partial thickness (Second Degree) Burn 75 75
Superficial (First Degree) Burn 25 25
No Clinical Signs, Symptoms or Conditions 19 19
Insufficient Information 11 11
Full thickness (Third Degree) Burn 5 5
Burn, Thermal 3 3
Patient Problem/Medical Problem 2 2
Injury 2 2
Erythema 2 2
Swelling 2 2
Electric Shock 1 1
Scarring 1 1
Blister 1 1
No Known Impact Or Consequence To Patient 1 1
Burning Sensation 1 1
Foreign Body In Patient 1 1
Numbness 1 1
Unspecified Tissue Injury 1 1
No Consequences Or Impact To Patient 1 1
Device Embedded In Tissue or Plaque 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Osteomed, LLC II Dec-06-2021
2 W&H DENTALWERK BUERMOOS GMBH II Feb-20-2024
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