55 results
·
21ms
·
Sources: EU EUDAMED, US FDA
IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235
FDA 510(k)
FDA Class 2
·Radiology
Oticon
FDA UDI
Oticon A/S·05707131167460·ACTO, ITC P L BE
Osstell SmartPeg Type 101
FDA UDI
Osstell AB·09010522002131·ISQ Measurement Peg
DEBAKEY AORTIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921007660·DEBAKEY AORTIC CLAMP CUP-SHAPED JAW ANGLED LEFT
WHITE TOE NAIL SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896049703·WHITE TOE NAIL SCISSORS
DEBAKEY AORTIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003323·DEBAKEY AORTIC CLAMP CUP-SHAPED JAW ANGLED LEFT
Ear Tip PM008 Pack/100 pcs. (Grason)
FDA UDI
PATH medical GmbH·04260223142079·PATH MEDICAL is not manufacturer or Labeler of ...
Disposable Accessories Kit
FDA UDI
RESTORATION ROBOTICS, INC.·00850470007081·
UA Impression Sleeve
FDA UDI
BICON, LLC·00813110027023·UA6 SP-TP Impression Sleeves (3)
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 18, 2015
SYNTHES (USA) LARGE FRAGMENT LOCKING COMPRESSION PLATE (LCP) SYSTEM-T PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
TRI-FIX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·August 3, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·August 4, 2015
INFINION 16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 17, 2018
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·October 8, 2015
MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2013
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·September 12, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·May 19, 2011
VA LOCKSCR Ø2.4 SELF-TAP L24 TAN
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 9, 2013