27 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Reprocessed Steerable Introducer
FDA 510(k)
FDA Class 2
·Cardiovascular
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063791·The blades and knifes consumables are for use w...
LEONE SPA
FDA UDI
LEONE SPA·08033707014171·CALIBRA 1ST MOL BANDS W/G8325-02 KIT UR
SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SPLASH! IMPRESSION MATERIAL DEVICE
FDA 510(k)
FDA Class 2
·Dental
QUADRA H CEMENTLESS STEM SIZE 3 LAT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·November 25, 2015
CERVSPINE-EXP-HEADSCR 4 SELF-DRILL L14
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KWQ·October 8, 2014
PROTECTA XT CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 7, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·July 7, 2011
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
HYBRID GLENOID BASE SMALL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 8, 2018
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·July 19, 2019
PTA BALLOON CATHETER(OHICHO3)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 13, 2017
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 14, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 30, 2020