FDA Adverse Event Malfunction Summary report: N

TMINI MINIATURE ROBOTIC SYSTEM

MDR report key: 23587189 · Received November 18, 2025

Report

Report Number
3000719653-2025-00016
Event Type
Malfunction
Date Received
November 18, 2025
Date of Event
October 16, 2025
Report Date
November 14, 2025
Manufacturer
THINK SURGICAL, INC
Product Code
OLO
UDI-DI
M9461093430
PMA / PMN Number
K252544
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

UPON INSPECTION OF THE RETURNED TMINI ROBOT, THINK SURGICAL, INC. CONFIRMED THAT ONE OF THE TWO THE NUT TUBES WAS BROKEN AND THE DOWEL PIN WAS MISSING. THE TMINI FUNCTIONED AS INTENDED AS ONLY ONE OF THE NUT TUBES WAS BROKEN. THINK SURGICAL REVIEWED THE DEVICE HISTORY RECORD AND CONFIRMED THERE WAS NO EVIDENCE OF DAMAGE TO THE NUT TUBE DURING PRODUCTION. THERE WAS NO INJURY TO PATIENT, AND THE SURGERY WAS COMPLETED WITHOUT COMPLICATION USING THE TMINI ROBOT. HOWEVER, THINK SURGICAL IS REPORTING THIS INCIDENT BECAUSE IF THE DOWEL PIN DETACHED DURING THE PROCEDURE, AND IT COULD POSE A RISK OF ENTERING THE SURGICAL INCISION.

Description of Event or Problem · 0

THE USER NOTICED A SMALL SILVER PIECE FALL OUT OF THE TMINI HEAD DURING STERILE SET-UP. DESPITE THIS, THE TMINI ROBOT WAS USED SUCCESSFULLY DURING THE PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1863271 TMINI MINIATURE ROBOTIC SYSTEM ORTHOPEDIC STEREOTAXIC INSTRUMENT OLO THINK SURGICAL, INC 109343 M9461093430

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown