62 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Smartinhaler
FDA 510(k)
FDA Class 2
·Anesthesiology
BI-METRIC XR-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304650510·
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768512·GENUMEDI PSS GREEN VII
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000455·MCK Patellofemoral Component
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376471266·Pad, Head Support
FUKUSHIMA SUCTION TUBE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896000346·FUKUSHIMA SUCTION TUBE
FUKUSHIMA SUCTION TUBE
FDA UDI
SONTEC INSTRUMENTS, INC.·B0991804070·FUKUSHIMA SUCTION TUBE
Ankle Clamp Strap
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063726·
N/A
FDA UDI
Ortho Development Corporation·00822409128952·4-in-1 Cut Guide w/ Anterior Lip Size 7
LIFE SPINE INTERSPINOUS FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BLACKSTONE SFS PARALLEL ROD CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024
ARTIS Q ZEEGO
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026
ARTIS ZEE III CEILING
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026
ARTIS ZEEGO III (CHINA)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 20, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·October 17, 2014