47 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Panorama Patient Monitoring Network
FDA 510(k)
FDA Class 2
·Cardiovascular
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486009366·MCK 12mm ONLAY INSERT SET
Oticon
FDA UDI
Oticon A/S·05707131284433·NERA2 PRO, DESIGNRITE 10 WL CBE DEMO
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100028·BLUMENTHAL SPECULUM X-HEAVY
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·August 10, 2017
Tibial Cutting Block 0deg (Left)
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215041359·
ENGAGE
FDA UDI
Smith & Nephew, Inc.·00885556875056·ANCHOR REMOVAL CHISEL
Engage Partial Knee System
FDA UDI
Engage UNI LLC·B6951500820000·Anchor Removal Chisel
GENPRIME DRUGS OF ABUSE READER SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CENTERPIECE PLATE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Engage Partial Knee System
FDA UDI
Engage UNI LLC·B695150082000A0·Anchor Removal Chisel
CENTERPIECE? PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code NQW·April 16, 2015
CENTERPIECE¿ PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·June 8, 2016
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·December 7, 2017
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code NQW·June 11, 2020
CENTERPIECE PLATE FIXATION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NQW·March 1, 2018