22 results · 21ms · Sources: EU EUDAMED, US FDA

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Proficient® Posterior Cervical Spine System

FDA 510(k)
FDA Class 2 ·Orthopedic

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776410667·Converse Scissors, 4 1/2", angled on flat

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741814400·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674181440060·

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X1814400·18mm H x 14mm W x 40mm L x 0 degrees XLIF

Integra® Miltex®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780361909·Integra® Miltex® Wilmer Conjunctival Scissors, ...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X18144080·18mm H x 14mm W x 40mm L x 8 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L181440120·18mm H x 14mm W x 40mm L XLIF Trial 12 degree L...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X181440120·18mm H x 14mm W x 40mm L x 12 degrees XLIF

Regatta Lateral System

FDA UDI
Seaspine Orthopedics Corporation·10889981158446·Lateral Implant, 18mm x 14mm x 40mm, 0 Deg

Regatta

FDA UDI
Seaspine Orthopedics Corporation·10889981158460·Lateral Implant, 18mm x 14mm x 40mm, 15 Deg

Regatta Lateral System

FDA UDI
Seaspine Orthopedics Corporation·10889981158453·Lateral Implant, 18mm x 14mm x 40mm, 10 Deg

BIVONA ADJUSTABLE AND FIXED NECKFLANGE HYPERFLEX TRACHEOSTOMY TUBES

FDA 510(k)
FDA Class 2 ·Anesthesiology

GMD UNIVERSAL URINARY INCONTINENCE SLING, MODEL 1012

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

LOOK

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAR·October 27, 2009

VC10 PUMP, 115V

FDA Adverse Event
Malfunction ·GYRUS ACMI, INC.·Product code HHK·January 2, 2025

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 21, 2013

CODMAN SURGICAL PATTIE

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC.·Product code HBA·July 11, 2011

530G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 17, 2014

RNGLC 32MM CONST 10DG LNR SZ14

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 29, 2016