29 results · 20ms · Sources: EU EUDAMED, US FDA

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IMDX FLU A/B AND RSV FOR ABBOTT M2000

FDA 510(k)
FDA Class 2 ·Microbiology

Sasmar Vanilla

FDA UDI
Sasmar Pharmaceuticals SPRL·09337213008266·PERSONAL LUBRICANT

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131584·TiBase ZS WP 1.5G E

TRANSEND GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

TRANSEND GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

TRANSEND GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

TRANSEND EX 14 GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009

SIROTORQUE L

FDA 510(k)
FDA Class 1 ·Dental

XYLOS MACRO-POROUS SURGICAL MESH

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

TRANSEND GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

TRANSEND GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

TRANSEND GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010

EZ BREATHE ATOMIZER

FDA Adverse Event
HEALTH & LIFE (SUZHOU) CO., LTD.·Product code CCQ·May 17, 2013

ACCU-CHEK ® SPIRIT COMBO

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·October 1, 2014

AUTOTOME RX SPHINCTEROTOME

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·June 16, 2011

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

smiths medical portex, Thermovent 1200, 15mm/22mm: a) REF 100/582/000; b) REF 100/582/000JP; c) REF 100/582/000JS

FDA Enforcement
Class II ·Ongoing·Smiths Medical ASD Inc.·October 30, 2024

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017