57 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100090·Tray Insert 2, Cosmolock, Arcamed
Navagio
FDA UDI
Kalitec Direct LLC·B07330K1100090·Tray Insert
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K1100090·Tray Insert, Level II
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1100090·Tray Insert
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 15, 2020
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·December 6, 2024
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075022934·KLEOS 2 PSL METAL MBT 022 LL12-LR12 PK5 UNI
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193108926·HA PEEK EVOS Straight, ,9mmx11mmx 26mm , FLAT ...
22mm x 10mm x 9mm PLIF with Inserter
FDA UDI
XENCO MEDICAL LLC·B064XM01100091·22mm x 10mm x 9mm PLIF
KOKO PEAK KP; KOKO PEAK KP+
FDA 510(k)
FDA Class 2
·Anesthesiology
SPACELABS PATHFINDER SL HOLTER ANALYZER
FDA 510(k)
FDA Class 2
·Cardiovascular
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 23, 2024
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS (TWO-LEVEL INDICATION)
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROTHESIS
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C® Cervical Disc Prosthesis
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·LDR Spine Mobi-C Cervical Disc Prosthesis
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·MOBI-C CERVICAL DISC PROSTHESIS