MAUDE Adverse Event Report: NAKANISHI INC. NSK; HANDPIECE, CONTRA- AND RIGHT-ANGLE ATTACHMENT, DENTAL

Model Number	Z95L
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Code	Partial thickness (Second Degree) Burn (2694)
Date of Event	01/29/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
On february 26, 2026, nakanishi became aware of handpiece overheating through a complaint input into the complaint database by a distributor (nsk america).Details are as follows: the event occurred on january 29, 2026.The dentist was performing a crown preparation procedure on a patient using the z95l handpiece (serial no.(b)(6).During the procedure, the handpiece overheated, and the patient received a thermal burn injury to their inner cheek.It was reported by the dental office that the patient's injury has healed normally without need for additional medical treatment.
Additional Manufacturer Narrative
The dental office declined to provide patient information for this event.
Additional Manufacturer Narrative
Upon receiving the device involved in the mdr event from the distributor, (b)(4) conducted a failure analysis of the returned device, which included measuring the operating temperature of the device [report no.(b)(4)].These activities are described in more detail below.Methodology used: a) (b)(4) examined the device history record and the repair history for the subject z95l device [serial no.(b)(6)].There were no problems observed during manufacturing or testing noted in the dhr.There were also no repair history records since the device was shipped.B) (b)(4) conducted temperature testing of the returned device in the following manner: b.1) temperature sensors were attached to the exterior of the device at various test points.This included the point most proximal to the patient (testing point (1)) and points further toward the distal end of the device (testing points (2) through (4)).The test setup was prepared to take temperature measurements at all points simultaneously, including a reference measurement at ambient room temperature.B.2) (b)(4) attached a thermocouple (sensor to measure temperature) to each of the testing points.(b)(4) rotated the device's motor at 40,000min-1, which is the maximum rpm for the motor that drives the handpiece (200,000min-1 for the handpiece), with water spray, and measured the exothermic response.B.3) (b)(4) measured the temperature rise of the returned handpiece set at 200,000min-1 (motor revolution 40,000min-1).(b)(4) observed rises in temperature at the test points as shown below; however, the temperatures were not high enough to cause a burn injury.The maximum temperatures during 5-minute temperature testing were as follows: - test point (1): 29.1 degrees c, - test point (2): 36.7 degrees c, - test point (3): 28.6 degrees c, - test point (4): 31.0 degrees c, identification of the specific failure mode(s) and/or mechanism(s) of the associated device components was conducted as follows: a) (b)(4) disassembled the handpiece and performed a visual inspection of the internal parts.(b)(4) observed the following: - the cartridge and the headcap were counterfeit.B) (b)(4) took photographs of all the disassembled parts and kept them in the investigation report no.(b)(4).Conclusions reached based on the investigation and analysis results: a) (b)(4) identified that the cause of the handpiece overheating was incorporation of the counterfeit cartridge and headcap.B) misuse by the user led to the handpiece overheating, which contributed to the reported event.D) in order to prevent the recurrence of the handpiece overheating, (b)(4) took the following actions: d.1) (b)(4) reviewed the operation manual and reconfirmed the clarity and understandability of the instructions.C) in order to prevent a recurrence of the handpiece overheating, (b)(4) took the following actions: c.1) (b)(4) reviewed the operation manual and reconfirmed the clarity and understandability of the instructions.C.2) (b)(4) reported the above evaluation results to the distributor and directed the distributor to remind the user of the importance of maintenance as instructed in the operation manual.

• Brand Name: NSK
• Common Device Name: HANDPIECE, CONTRA- AND RIGHT-ANGLE ATTACHMENT, DENTAL
• Manufacturer (Section D): NAKANISHI INC.; 700 shimohinata; kanuma-shi, tochigi-ken 322-8 666; JA 322-8666
• Manufacturer (Section G): NAKANISHI INC.; 700 shimohinata; kanuma-shi, tochigi-ken 322-8 666; JA 322-8666
• Manufacturer Contact: sean kaufman ; 1800 global parkway; hoffman estates, IL 60192 ; 2245128921
• MDR Report Key: 24636011
• Report Number: 9611253-2026-00010
• Device Sequence Number: 9014978
• Product Code: EGS
• UDI-Device Identifier: 04560264575448
• UDI-Public: (01)04560264575448
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• PMA/510(K) Number: K202960
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative,Distributor
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/22/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: Z95L
• Device Catalogue Number: C1034
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/12/2026
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/26/2026
• Supplement Date Received by Manufacturer: 04/09/2026
• Initial Report FDA Received Date: 03/19/2026
• Supplement Report FDA Received Date: 04/22/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/12/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown