144 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Nextra CH Cannulated Hammertoe System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221610000·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221610070·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221610150·
BD BBL™ Brain Heart Infusion Agar Slant
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902216101·BD BBL™ Brain Heart Infusion Agar Slants, Packa...
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981215538·No-Profile Interbody, 39mm x 27mm x 16mm, 10 Deg
COBAS C 501 TINA-QUANT HBA1CDX GEN.3 ASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
QAB2A IGM ELISA KIT HRP
FDA 510(k)
FDA Class 2
·Immunology
J & J INSTRUMENTS
FDA UDI
J & J INSTRUMENTS INC·00817524025705·MAYO SCISSOR 6.75"" STR
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730086211·TruFit™2.0 .022 MC UR6 CONV SBT -14T 10DO WLD (...
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730085559·Trufit™ 2.0 .022 MC UR6 CONV SBT -14T 10DOff DB...
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468083328·Interbody Fusion Device, 22mm (W), 16mm (D), 10...
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468083397·Interbody Fusion Device, 22mm (W), 16mm (D), 10...
INTEGRAL/XLAT POR PROFILE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·January 29, 2019
BLACKHAWK Cervical Spacer System
FDA UDI
Choice Spine, LP·00840996164641·BLACKHAWK,STERILE,PARALLEL,16X14X10
Unison®-C Anterior Cervical Fixation System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468081713·Trial, 22mm (W), 16mm (D), 10mm (H), 7° Lordosis
GREENLIGHT XPS LASER SYSTEM
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·November 3, 2014
SMART TOE ANGLED 16MM
FDA Adverse Event
Injury
·MEMOMETAL TECHNOLOGIES SA·Product code HTY·August 19, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 11, 2013
M2A-MAGNUM MOD HD SZ 50MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·August 9, 2018