26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Foot and Ankle System
FDA 510(k)
FDA Class 2
·Orthopedic
MaXcess
FDA UDI
Nuvasive, Inc.·00887517075826·MaXcess Access Kit, Shim Small
IBP Interface cable (MX980 - Medex 980)
FDA UDI
MIPM Mammendorfer Institut für Physik und Medizin GmbH·EMIP52000620·
IBP Interface cable (MX980 - Medex 980)
FDA UDI
MIPM Mammendorfer Institut für Physik und Medizin GmbH·04255629200669·
STEVENS TENOTOMY SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896054363·STEVENS TENOTOMY SCISSORS STRAIGHT LONG BLUNT B...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005890·1.3mm Pilot Drill, J-Latch, 16mm
BROLI-ADSON FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896084469·BROLI-ADSON FORCEPS STRAIGHT TUNGSTEN CARBIDE D...
Drill Guide
FDA UDI
Treace Medical Concepts, Inc.·00810111221535·Staple Drill Guide
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 18, 2014
OsteoMed
FDA UDI
OSTEOMED LLC·00845694066242·1.6 System 1.3mm Pilot Drill 16mm J-Latch Steri...
XERAFIT
FDA 510(k)
FDA Class 2
·Dental
CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
ML TAPER SZ15.0 EXT OFFSET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·October 12, 2021
INTERSTIM
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 15, 2008
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIM·August 10, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 1, 2013
SMR SHOULDER
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·July 18, 2024
ECCENTRICAL GLENOSPHERE DIA. 40 MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code MBF·December 19, 2022
Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic
FDA Recall
Terminated
·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013
FEMORAL HEAD 0X36MM DIA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·July 22, 2021