10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES (USA) 3.5MM CONICAL SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450047170·
CT LUCIA
FDA UDI
CARL ZEISS MEDITEC PRODUCTION, LLC·00843045101048·3-piece, monofocal, hydrophobic, acrylic, intra...
ISOROD PD-103 IMPLANT, MODEL ATI-PD-103
FDA 510(k)
FDA Class 2
·Radiology
MODIFIED SINGLE AXLE TOTAL ELBOW
FDA 510(k)
FDA Class 2
·Orthopedic
BARD-PARKER CARBON RIB-BACK BLADES SIZE 11, STERILE
FDA Adverse Event
Injury
·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code GES·February 22, 2018
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 10, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 2, 2014
RIATA PASSIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
ANKLE FUSION PLATE, LATERAL TTC
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRS·July 22, 2020