23 results
·
24ms
·
Sources: EU EUDAMED, US FDA
SPINEMED
FDA 510(k)
FDA Class 2
·Physical Medicine
Invotec Silicone Sheeting
FDA UDI
INVOTEC INTERNATIONAL, INC.·00818501021291·Invotec Silicone Sheeting 12 x 12 x 0.060"
SCFE Screw
FDA UDI
ORTHOPEDIATRICS CORP.·00841132114292·4.0mm X 60mm MED THREAD CANNULATED SCREW
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933363·Percutaneous Transluminal Angioplasty Balloon C...
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981174811·Z-Rod, Dia. 5.5mm, Titanium, 60mm
Citrelock ACL 6mm Femoral Drill Guide
FDA UDI
Acuitive Technologies, Inc.·00810027271020·
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933974·Percutaneous Transluminal Angioplasty Balloon C...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710420300600·Anterio Lateral Closing Wedge Osteotomy Guide, ...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710410300600·Anterior Closing Wedge Osteotomy Guide, 30mm x ...
GEL MARK BIOPSY SITE MARKER, MODELS MKOOO1, MK0004, MK0007
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PLASMAKINETIC GENERATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
"ACORN BUR, TOOLSTEEL, LONG"
FDA Adverse Event
Malfunction
·STRYKER IRELAND LTD·Product code HBE·November 19, 2009
UNIVERSAL CLAMP STAINLESS STEEL SYSTEM, MODELS SNA027-0-30060, SNA027-0-30063
FDA 510(k)
FDA Class 2
·Orthopedic
1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER
FDA Adverse Event
Injury
·SYNTHES USA·Product code JEY·November 2, 2012
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 4, 2025
5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/80MM
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·April 2, 2013
COULTER® HMX AUTOLOADER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code GKZ·March 25, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·April 15, 2008
ASSEMBLY-ROTARY SCALE: 190-00126
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·January 2, 2019
ANSPACH INTEGRATION PACKAGING ASSEMBLY
FDA Adverse Event
Malfunction
·MAKO SURGICAL CORP.·Product code OLO·March 19, 2019