259 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
GLADIATOR HIP STEM
FDA 510(k)
FDA Class 3
·Orthopedic
POLYPERF SAFE
FDA UDI
PEROUSE MEDICAL·03661234014125·
SOL-M™ Hypodermic Needle
FDA UDI
Sol-Millennium Medical, Inc.·00818392015447·Sterile hypodermic needles intended to inject f...
MAXCUT CARBIDE BUR (100/pk) FG 4
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77811119101·MAXCUT CARBIDE BUR (100/pk) Shape: Round; Size:...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111211591·HENNIG PLAST SPREADER 2BLD 11"
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000110·11mm LG Fixed 10° Lordotic, HiJAK™ Cervical
Trocar
FDA UDI
SOPRO-COMEG GmbH·04059082005386·
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000140·14mm LG Fixed 10° Lordotic, HiJAK™ Cervical
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000120·12mm LG Fixed 10° Lordotic, HiJAK™ Cervical
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000100·10mm LG Fixed 10° Lordotic, HiJAK™ Cervical
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000130·13mm LG Fixed 10° Lordotic, HiJAK™ Cervical
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000080·8mm LG Fixed 10° Lordotic, HiJAK™ Cervical
HiJAK™ Cervical
FDA UDI
ATLAS SPINE, INC.·M68111191000090·9mm LG Fixed 10° Lordotic, HiJAK™ Cervical
IN-FAST BONE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
3M ATTEST RAPID READOUT STEAM PROCESS CHALLENGE DEVICE, MODEL 1296V, 3M ATTEST RAPID READOUT STEAM-PLUS
FDA 510(k)
FDA Class 2
·General Hospital
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025
EMAX 2 PLUS MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·May 7, 2013
ASCENSIA CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·August 8, 2008
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 2, 2011