36 results
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30ms
·
Sources: EU EUDAMED, US FDA
HELIODENT VARIO
FDA 510(k)
FDA Class 2
·Dental
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65890006721·FILES HEDSTROM #15 21MM
CUSTOM PROCEDURE KIT
FDA UDI
MEDIVATORS INC.·40677964006041·CUSTOM PROCEDURE KIT
Implant Prosthetics
FDA UDI
Preat Corporation·00842092117422·NobelBiocare™ Tri-Lobe-compatible WP Esthetic A...
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040094164·Maxima Hedstrom Files 21mm
Isolator Surgical Ablation System
FDA UDI
ATRICURE, INC.·00818354016352·Glidepath Tape (1-Unit)
APPLIANCE, FIXATION, NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·August 18, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 5, 2016
DORNIER MEDILAS D SKINPULSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEPUY CONTOUR UNICOMPARTMENTAL KNEE PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES BETTLACH·Product code HWC·September 23, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES MEZZOVICO·Product code HWC·September 1, 2015
LCP 4.5/5 BROAD 18HO L332 TI
FDA Adverse Event
Injury
·SYNTHES·Product code KTT·December 12, 2012
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·March 12, 2013
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIM·February 24, 2011
LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·February 19, 2008
LOCKSCR Ø5 SELF-TAP L55 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·April 11, 2013
LOCKSCR Ø5 SELF-TAP L40 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·June 27, 2013
LINEAR 3-6
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 20, 2023
LOCKSCR Ø5 SELF-TAP L44 TAN
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code KTT·October 18, 2013