21 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SERRATED GRASPING FORCEPS, CURVED DOWN
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668108970·ARBISSER ANTERIOR CHAMBER CANNULA 27GA
Arthrex®
FDA UDI
ARTHREX, INC.·00888867288270·Low Profile Screw,Cortical,3.5x10mm,DRP
ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BioStamp nPoint
FDA 510(k)
FDA Class 2
·Cardiovascular
MICRO RECIPROCATING SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·October 14, 2010
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·December 14, 2012
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014
2.4 X 18MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW,LOCKING,3.5X12MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW,CORTICAL,3.5X10MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
2.4 X 18MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW,LOCKING,3.5X14MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW,CORTICAL,3.5X14MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW,CORTICAL,3.5X11MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
VOLAR DISTAL RAD PLT TI NARROW LT 3H
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
LOW PROFILE SCREW, 2.4 X 18MM, CORTEX
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·August 27, 2020
LOW PROFILE SCREW,CORTICAL,3.5X13MM,DRP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
2.4 X 16MM VAL SCREW, TI
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·August 27, 2020
XP-XP Tibial Tray - Interlok 67 mm Item # 195753
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019