MAUDE Adverse Event Report: DENTSPLY LLC CAVITRON 300 SERIES 115VDOM(DNA); SCALER, ULTRASONIC

Catalog Number	8270310
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Since an overheating insert could necessitate medical/surgical intervention to preclude permanent damage to a body structure or permanent impairment of a body function, this malfunction would be likely to cause/contribute to a serious injury should it recur.As such, this event meets the criteria for reportability per 21 cfr part 803.The device is available for evaluation, though has not been returned as of this report.Evaluation results will be submitted as they become available.
Event or Problem Description
While the customer was using a cavitron 300 series g310 they allege that the insert heats up.No injury was reported from the alleged event.
Additional Manufacturer Narrative
Within warranty? no.Serial number: (b)(6).Notes: will call back with email when they get the replacement for the label (b)(6) (b)(6) 2026 replaced on 31263851 (b)(6).Repair tech: (b)(6) 000 evaluated, meets specifications, contact customer no fault found, unit working with company specs.Footswitch was low on charge.Dhr review is not required because the product was returned for evaluation.The service technician could not replicate the failure noted in the complaint with the returned unit.No additional action is necessary.

• Brand Name: CAVITRON 300 SERIES 115VDOM(DNA)
• Common Device Name: SCALER, ULTRASONIC
• Manufacturer (Section D): DENTSPLY LLC; 1301 smile way; york PA 17404
• Manufacturer (Section G): DENTSPLY LLC; 1301 smile way; york PA 17404
• Manufacturer Contact: dan eagar ; 221 w. philadelphia st.; york, PA 17401 ; 7178494593
• MDR Report Key: 23903718
• Report Number: 2424472-2025-00169
• Device Sequence Number: 9389241
• Product Code: ELC
• UDI-Device Identifier: D00382703101
• UDI-Public: D00382703101
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K150535
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup
• Report Date (Section B): 01/30/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 8270310
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 12/16/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/28/2025
• Supplement Report FDA Received Date: 01/30/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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
• Patient Sequence Number: 1
• Patient Sex: Unknown