36 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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