17 results
·
24ms
·
Sources: EU EUDAMED, US FDA
TruDiagnosis System
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304271500·
MICRO TRAY
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896019560·MICRO TRAY DOUBLE LEVEL WITH PIN MAT/RETAINERS ...
Avalign
FDA UDI
Avalign Technologies, Inc.·00190776022945·Microsurgical Case two level
ELMED
FDA UDI
ELMED INCORPORATED·00842180185487·RENAL VEIN FIXED RETRACTOR, 1" X 8"
ZOLL IVTM QUATTRO CATHETER
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION INC·Product code NCX·August 15, 2023
ULTRASONIC SCALER
FDA 510(k)
FDA Class 2
·Dental
SPIRODOC
FDA 510(k)
FDA Class 2
·Anesthesiology
REVERSE SHOULDER SYSTEM 04.01.0110 HUMERAL REVERSE METAPHYSIS +0MM/0
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·October 1, 2021
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+6MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·February 13, 2020
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·Product code OYC·October 18, 2014
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Malfunction
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011
T2 STRATOSPHERE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MQP·July 1, 2020
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code ELC·April 29, 2020
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code ELC·May 31, 2023
XP-XP Tibial Tray - Interlok 73 mm Item # 195756
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019