5 results
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63ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code OLO·April 11, 2014
Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code KKX·July 19, 2013
CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
FDA Recall
Open, Classified
·Blue Belt Technologies, Inc·Product code OLO·November 13, 2023
CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT - UNIVERSAL.Intended to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures Product Numbers: (1) ROB10000 CORI Starter Kit (2) ROB10024 Real Intelligence CORI (3) ROB10197 CORI STARTER KIT - UNIVERSAL Note: the three product numbers cover the three different configurations in which the CORI Console is sold
FDA Recall
Open, Classified
·Blue Belt Technologies, Inc·Product code OLO·May 7, 2024
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299
FDA Recall
Open, Classified
·Blue Belt Technologies, Inc·Product code OLO·September 7, 2023