23 results · 24ms · Sources: EU EUDAMED, US FDA

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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