27 results · 30ms · 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.

SOVEREIGN SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

Innospire Deluxe

FDA UDI
VEGA TECHNOLOGIES INC.·06946159502047·1110063

STRIDE Unicondylar Knee

FDA UDI
BLUE BELT TECHNOLOGIES, INC.·00841153100403·STRIDE Femoral Implant SIZE 1 LM/RL

LARGE CANNULATED SCREWS

FDA UDI
Smith & Nephew, Inc.·03596010033574·TRAY/CASE FOR CANNULATED HIP PINS

SCISSORS METZENBAUM STR 7"

FDA UDI
W.H. Holden, Inc.·D9281100630·

Leva® Anterior Interbody System

FDA UDI
Spine Wave, Inc.·10840642108644·Modular Spacer, SSA, 26 mm (W) x 26 mm (L) x 9 ...

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws

Avalign

FDA UDI
Avalign Technologies, Inc.·00190776021306·Slotted U Bracket

Innomed, Inc.

FDA UDI
INNOMED, INC.·00840277119933·Flexible Headed and Straight Pin Puller

NA

FDA UDI
STRYKER CORPORATION·04546540990396·1.7mm Steiger Carbide Fissure

HYPERFORM OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER MODEL

FDA 510(k)
FDA Class 2 ·Cardiovascular

COUCH FOR TOTAL BODY RADIATION

FDA 510(k)
FDA Class 2 ·Radiology

RESPIRONICS

FDA Adverse Event
Malfunction ·Product code MNT·April 8, 2021

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 26, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·May 13, 2013

APEX OVER-THE-WIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·June 1, 2011

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·August 14, 2008

EQUINOXE SHOULDER COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWS·January 9, 2024