255 results · 26ms · Sources: EU EUDAMED, US FDA

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A-TONE IPL SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Bernafon

FDA UDI
Bernafon AG·05711584049600·PC9 N, PS SF GR PRECISO 9

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131712·AngBase MA NE

Pro-Link Ti

FDA UDI
Life Spine, Inc.·00190837080723·

ELMED

FDA UDI
ELMED INCORPORATED·00198506058615·forceps tissue, BONNEY, 1x2 teeth, 18cm

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158210462·FORCEPS BONNEY TISSUE 1X2 TEETH SERRATED 7"

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311317120·

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321317120·

ALEUTIAN® Interbody Systems

FDA UDI
VB Spine LLC·10888857561717·Trial Size 13x16x8 mm, 7 Deg.

INION OTPS BIODEGRADABLE PIN

FDA 510(k)
FDA Class 2 ·Orthopedic

ENDOVASCULAR LAER VEIN SYSTEM KIT

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 29, 2013

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

PERCLOSE A-T SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·June 16, 2011

COOK CELECT PLATINUM NAVALIGN JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·September 12, 2019

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·January 29, 2020

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·March 31, 2020

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·September 19, 2019

GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·February 23, 2022

COOK CELECT PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·February 27, 2021