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

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Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·CRYOCOR CRYOABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·CRYOCOR CRYOABLATION SYSTEM

EASYLIFE

FDA UDI
Respironics, Inc.·00606959001329·Large EasyLife Mask with Headgear, China

Ni-Ti - Archwire

FDA UDI
ORMCO CORPORATION·00889989025354·PREF.LING.ARCH NI-TI UP18 SZ2 PK/10

Humelock II Cemented Reversible Shoulder

FDA UDI
FX SOLUTIONS·03701037300237·HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEP...

Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW

FDA UDI
Osteocentric Technologies, Inc.·00816950026690·Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710300500240·Tibial Osteotmy Guide, 50mm x 24mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710420500240·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710400500240·Anterior Dome Osteotomy Guide, 50mm x 24mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710410500240·Anterior Closing Wedge Osteotomy Guide, 50mm x ...

ONE STEP MULTIPLE DRUGS OF ABUSE ASSAYS

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

PORTEX CO2 CLIP

FDA Adverse Event
Death ·SMITHS MEDICAL ASD, INC.·Product code CCK·November 9, 2005

HUMELOCK REVERSED SHOULDER

FDA Adverse Event
Injury ·FX SOLUTIONS·Product code PHX·June 21, 2019

Qualitative And Quantitative Hepatitis B Virus Antibody Assays

FDA Pre-Market Approval
FDA Class 2 ·VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC REAGENT PACK/CALIBRATOR

Occluder, Patent Ductus, Arteriosus

FDA Pre-Market Approval
FDA Class 3 ·AMPLATZER DUCT OCCLUDER AND 180 DEGREE DELIVERY SYSTEM

HUMELOCK REVERSED SHOULDER

FDA Adverse Event
Injury ·FX SOLUTIONS·Product code PHX·July 9, 2019

RESTYLANE INJECTABLE GEL

FDA Adverse Event
Other ·Q-MED AB·Product code LMH·April 13, 2012

RESTYLANE INJECTABLE GEL

FDA Adverse Event
Other ·Q-MED AB·Product code LMH·May 16, 2008

RESTYLANE INJECTABLE GEL

FDA Adverse Event
Other ·Q-MED AB·Product code LMH·March 29, 2007

RESTYLANE INJECTABLE GEL

FDA Adverse Event
Other ·Q-MED AB·Product code LMH·April 14, 2011