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

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STRYKER SPINE REFLEX TRANSLATIONAL ANTERIOR CERVICAL PLATING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Non-Locking Screw, 2.7mm x 20mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665026320·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694008679·3.0mm x 20mm Lag Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694035248·3.0 x 20mm Lag Screw, Sterile

MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0130201·PLATE CALIPER

Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K0380200·Handle, Threaded Standard Dynamo

OsteoMed

FDA UDI
OSTEOMED LLC·00845694067522·3.0 x 20mm Lag Screw Sterile Qty 5

CARDIAC FUNCTION LABORATORY; PRESSURE INTERFACE; PRESSURE / VOLUME CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTE

FDA 510(k)
FDA Class 2 ·Radiology

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

SINAI HSP BALTIMORE MD 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DTZ·July 6, 2011

ADVIA CENTAUR CKMB AND TROPONIN ULTRA ASSAY

FDA Adverse Event
Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JHX·July 29, 2010

LAKELAND REG LAKELAND FL 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWF·May 3, 2010

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

WA ADVENT TAKOMA PARK MD 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011

ACCU-CHEK ® COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·April 29, 2013