11 results · 19ms · Sources: EU EUDAMED, US FDA

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CSF-VENTRICULAR CATHETER, STANDARD DES

FDA 510(k)
FDA Class 2 ·Neurology

Safco T&F Bur - 12 Bladed

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72327920073·Safco T&F bur - 12 bladed, carbide, #7104 flame...

Coblation

FDA UDI
Smith & Nephew, Inc.·00817470004472·PERC DLR SPINE WAND SURGICAL DEVICE

SpineWand

FDA UDI
MORGAN STEER ORTHOPAEDICS LIMITED·05060696460002·Perc DLR Convenience Pack Inc 17 gauge 6” Crawf...

Continuum® Trilogy® IT Allofit® IT Acetabular Systems

FDA UDI
Zimmer, Inc.·00889024152809·

TheraBase, TheraBase Ca

FDA 510(k)
FDA Class 2 ·Dental

ROTARY SCALER

FDA 510(k)
FDA Class 2 ·Dental

OCTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code GZB·October 12, 2012

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2014

AUTOSUTURE PREMIUM SURGICLIP SMALL 9.0

FDA Adverse Event
Malfunction ·COVIDIEN·Product code GDO·August 4, 2010

Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407, 60010741-707; CD1211-36/100006983, 100012542, 100016679, 100031495, 100035634, 100035635, 100042587, 100047090; CD1211-36Q/100004079, 100004081, 100019783, 100035607, 100042591, 100047191; CD1215-36/100006990, 100010230, 100010241, 100010242, 100010244, 100012563, 100012564, 100034631, 100046574, 100046786; CD1215-36Q/100006768, 100006769, 100006770, 100023300, 100030306, 100033794, 100042402, 100046720, 100046904; CD1217-36/100011824; CD1219-36/100002160, 100002864, 100011826; CD1219-36Q/100004071, 100023301; CD2211-36/100006982, 100012536, 100016678, 100031440, 100035629, 100035636, 100042520, 100047192; CD2211-36Q/100004085, 100004087, 100019782, 100035587, 100042575, 100047193; CD2215-36/100006992, 100010224, 100010226, 100010227, 100010228, 100012515, 100012516, 100036606, 100046676, 100046792, 60019063; CD2215-36Q/100006762, 100006763, 100006764, 100023302, 100029180, 100033793, 100042404, 100046789, 100046905; CD2217-36/100011828, 100046991, 60016124-401; CD2219-36/100002139, 100002140, 100002862, 100011830; CD2219-36Q/100023303

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018