16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HIGH V+
FDA 510(k)
FDA Class 2
·Orthopedic
Ceramco® II Silver™
FDA UDI
Dentsply International Inc.·D0011611140·
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306820496·Babcock Baby Forceps, 13.5cm
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916157265·ZEUS®-L CUP CURETTE, STRAIGHT, STRAIGHT TIP 4MM
Symmetry Rochester-Pean
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482040270·Symmetry® Forceps, Rochester-Pean Hemostatic, C...
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837059590·Plateau-X Installer
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167521611140·
SURESIGNS VS2+ NBP/SPO2/WIRELESS
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code MHX·August 26, 2021
ADVANCIS ACTIVON TUBE
FDA 510(k)
FDA Unclassified
·Unknown
WDS, SIZE 2 AND SIZE 2
FDA 510(k)
FDA Class 2
·Dental
MALLORY/HEAD - PF ACETABULAR COMPONENT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·March 8, 2017
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
RESTORE PRIME
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 17, 2011
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·October 10, 2014
ANATOMIC
FDA Adverse Event
Malfunction
·AMPLITUDE·Product code JWH·December 11, 2018
Glidesheath Slender Hydrophilic Coated Introducer Sheath, 6FR - 10CM (0.021), REF/Product Code RM*RS6F10PA, STERILE, Rx ONLY
FDA Enforcement
Class II
·Terminated·Terumo Medical Corp·December 20, 2017