3,637 results · 22ms · Sources: EU EUDAMED, US FDA

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iTEMPSHIELD

FDA 510(k)
FDA Class 2 ·General Hospital

OptoMonitor 3

FDA UDI
Opsens Inc·07540184320103·

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580382·Rod(CoCr), Ø5.5 x 100mm

LEONE SPA

FDA UDI
LEONE SPA·08033707066804·ELASTIC LIGATURES TRANSP 1,0mm

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981247386·No-Profile Interbody, 39mm x 30mm x 20mm, 10 Deg

SPEEDLOCK

FDA UDI
Smith & Nephew, Inc.·00817470002935·SPEEDLOCK HIP DRILL

Smith and Nephew

FDA UDI
Provision·B504OM2320100·

Sapphire NC ULTRA Coronary Dilatation Catheter

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955982323·

TSI Stem Broach

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215040451·

MABIS

FDA UDI
D-M-S HOLDINGS, INC.·00767056232013·CALIBER ANEROID GAUGE BLUE

SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020

FDA 510(k)
FDA Class 2 ·Orthopedic

VIDAS C DIFFICILE GDH

FDA 510(k)
FDA Class 1 ·Microbiology

GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILE

FDA 510(k)
FDA Class 1 ·General Hospital

INFUSOR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·September 1, 2011

ROTATING MULTIPLE CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·November 6, 2014

DUROM US ACETABULAR COMPONENT 50/44 J

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·July 4, 2013

UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·August 19, 2011

Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications.

FDA Enforcement
Class II ·Terminated·Baxter Healthcare Corp.·July 3, 2013

OPTI-FREE REPLENISH

FDA Adverse Event
Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·September 3, 2010

OPTI-FREE REPLENISH

FDA Adverse Event
Injury ·ALCON - FORT WORTH / ALCON LABS INC·Product code LPN·September 1, 2010