10 results
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21ms
·
Sources: EU EUDAMED, US FDA
STERILE SUTURE REMOVAL KIT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Pro Advantage Buffered Iontophoresis Electrode Treatment Kit
FDA UDI
NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P8503252·Gentle Stim Ionto Buffered Iontophoresis Electr...
DD base P HI
FDA UDI
Dental Direkt GmbH·EDDIK503251·DD medical polymers (PMMA), made from PMMA, are...
AngioSystems Tray
FDA UDI
ANGIOSYSTEMS, INCORPORATED·00816611026397·
Range/Denali/Mesa Spinal System
FDA 510(k)
FDA Class 2
·Orthopedic
DISPOSABLE CONCENTRIC PROBE, DISPOSABLE BIPOLAR PROBE, DISPOSABLE MONOPOLAR PROBE
FDA 510(k)
FDA Class 2
·Neurology
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 30, 2014
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 26, 2012
TWIST DRILL FOR 4MM SCREWS, DIAM.0.9X46MM, WL5.3M
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS FREIBURG·Product code HBE·September 22, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015