95 results · 21ms · Sources: EU EUDAMED, US FDA

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MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0600010·Tray Insert, Level 1

Ocata Anterior Cervical System

FDA UDI
Kalitec Direct LLC·B07308K0600010·Tray Insert 1, Ocata

D-10 HEMOGLOBIN A1C PROGRAM; D-10 DUAL PROGRAM

FDA 510(k)
FDA Class 2 ·Hematology

HI-TORQUE COMMAND™

FDA UDI
ABBOTT VASCULAR INC.·08717648356810·HI-TORQUE COMMAND™ 14 ST Guide Wire with Hydrop...

Ormco

FDA UDI
ORMCO CORPORATION·00889989026283·ARCH LING SST 16 DIA PK 10

n/a

FDA UDI
Ortho Development Corporation·00822409074594·Greater Trochanter Reamer

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481125294·Locator F-Tx Abutment for 3.0 Internal Hex Conn...

Niobe MNS Siemens

FDA UDI
Stereotaxis, Inc.·M58800100600010·Stereotaxis Niobe Magnetic Navigation System (M...

LIVESURE THC SCREEN TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·January 13, 2016

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·January 13, 2016

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·January 13, 2016

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·PROTEGE GPS AND PROTEGE RX CAROTID STENT SYSTEMS

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 13, 2016

3.2MMX30MM RNGLC+ ACET DRL BIT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HTW·January 26, 2023

ALARIS PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FPA·March 19, 2013

PULSE GEN MODEL 102

FDA Adverse Event
Malfunction ·CYBERONICS, INC.·Product code LYJ·June 10, 2008

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 15, 2011

3.2MMX30MM RNGLC+ ACET DRL BIT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HTW·January 26, 2023