290 results · 23ms · 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.

Cogent Hemodynamic Monitoring System

FDA 510(k)
FDA Class 2 ·Cardiovascular

LEONE SPA

FDA UDI
LEONE SPA·08033707013860·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 6

BLUEENDO

FDA UDI
TROKAMED GmbH·04251303824978·Obturator Ø 15 mm for complete system to be use...

Geneva

FDA UDI
Nucletron B.V.·08717213056015·Interstitial Tube

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613053611·ID Instrument Sheet Tape, Solid, Purple, 8-1/2"...

Stryker

FDA UDI
Provision·B504OM21081520060·

NA

FDA UDI
STERILMED, INC.·10888551036276·SAW BLADE SAGITTAL SPECIAL BLADE CONVERSION SYS...

Speed Shift

FDA UDI
Synthes GmbH·00810633020425·Speed Shift 15x20x20 Offset 6mm Implant

Stryker

FDA UDI
Provision·00810041633767·

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613057671·Abdominal Spatula, 6mm Wide, Maleable, Overall ...

NA

FDA UDI
STRYKER CORPORATION·04546540939531·2108 Series Sagittal Blade, Ground (12.5 x 0.89...

CRYOMEGA

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

POWDER-FREE VINYL EXAM GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

Herbert/Whipple®

FDA UDI
Zimmer, Inc.·00889024033788·

MICROAIRE

FDA Adverse Event
Injury ·MICROAIRE SURGICAL INSTRUMENTS·Product code HRX·October 11, 2006

ACRYSOF

FDA Adverse Event
Injury ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·November 17, 2006

HIRES 90K

FDA Adverse Event
Injury ·ADVANCED BIONICS CORPORATION·Product code MCM·April 10, 2006

NEXGEN COMPLETE KNEE SOLUTION LEGACY KNEE-CONSTRAINED CONDYL

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·March 29, 2006

BD LUER-LOK¿ TIP SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·September 14, 2022

CONTAK RENEWAL

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·February 8, 2007