54 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AOS 6.5MM CAPTURED, FULLY THREADED CANCELLOUS SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868558641·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868247927·
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·08428898831230·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T1412280·14mm TLIF Implant 12mm Wide 28mm Length
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T14122870·14mm TLIF Implant 12mm Wide 28mm Length 7 Degrees
MIRADA XD
FDA 510(k)
FDA Class 2
·Radiology
MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200
FDA 510(k)
FDA Class 2
·Cardiovascular
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151702·14 X 12 CERVICAL TRIALS 28MM 10° LORDOSIS
INCORPORATE
FDA UDI
SPINAL ELEMENTS·00840606151511·14 X 12 CERVICAL TRIALS 28MM 0° LORDOSIS
PFNA-II BLADE L85 TAN
FDA Adverse Event
Malfunction
·SYNTHES (USA·Product code LXT·June 3, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 27, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 3, 2014
VANGUARD ARCOM POSTERIOR STABILIZED BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018
VANGUARD PS+ TIB BRG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
VAN PS OPEN INTL FEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021
HF UNIT "ESG-400"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·December 5, 2017
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 8, 2020
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·November 17, 2020