30 results · 26ms · Sources: EU EUDAMED, US FDA

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STRATAFIX Spiral MONOCRYL Knotless Tissue Control Device, STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control Device

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169524729·SHAFT 2151200 THREADED SHAFT

POUR-PLUS

FDA UDI
Denplus Inc·D8451151200·POUR-PLUS, CLR, 2.3 kg

SimPro™ Now

FDA UDI
Wellspect AB·07392532188947·Single Use Urinary Catheter with water sachet. ...

SimPro™ Now

FDA UDI
Wellspect AB·07333387032719·Single Use Urinary Catheter with water sachet. ...

AOS CLAMP 9.5mm ROD x 9.5mm ROD

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665005387·

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690192336·Revision Knee Reamer Spiral Fluted - Zimmer 20mm

TALOS®-C HA

FDA UDI
MEDITECH SPINE, LLC·B167521512000·

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702580044·ELVAREX 1/THIGH HIGH/SLANT-CLOSED TOE/DOTTED 2,...

HEMOGLOBIN A1C REAGENT SET

FDA 510(k)
FDA Class 2 ·Hematology

PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·July 29, 2020

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·July 28, 2020

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·July 28, 2020

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 27, 2023

ACCU-CHEK ACTIVE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·March 11, 2009

GMK-REVISION FIXED TIBIAL INSERT SC # 4/14MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 27, 2018

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

PINNACLE 100 ACET CUP 56MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 30, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008