50 results · 24ms · 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.

COHEN CROSSOVER CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X1016250·10mm H x 16mm W x 25mm L x 0 degrees XLIF

Novo Surgical

FDA UDI
NOVO SURGICAL, INC.·00842331190674·double-ended probe, stainless steel, 5-1/2" (14...

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981265519·Trial, 31mm x 24mm x 16mm, 25 Deg

Orthoquest

FDA UDI
Young Innovations, Inc.·00843471133859·T D-Form 019X025

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981246273·Interbody, 31mm x 24mm x 16mm, 25 Deg

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L101625120·10mm H x 16mm W x 25mm L XLIF Trial 12 degree L...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X101625120·10mm H x 16mm W x 25mm L x 12 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X10162580·10mm H x 16mm W x 25mm L x 8 degrees XLIF

Young Specialties

FDA UDI
Young Innovations, Inc.·00840326426159·NiTi Thermal Archwire, D-Form .019x.025 10EA

FacetLink System

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575081493·Facet Screw

OVUM ASPIRATION NEEDLE SINGLE LUMEN

FDA Adverse Event
Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 19, 2018

PRONOVA NONABSORBABLE SUTURE, USP

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

VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)

FDA 510(k)
FDA Class 2 ·Cardiovascular

FEMORAL POSTERIOR AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

OVUM ASPIRATION NEEDLE SINGLE LUMEN

FDA Adverse Event
Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 22, 2018

STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

FEMORAL DISTAL AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

TIBIAL AUGMENT CEMENTED HALF BLOCK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

FEMORAL DISTAL AUGMENT CEMENTED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022