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

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STARLIGHT

FDA 510(k)
FDA Class 2 ·Neurology

N/A

FDA UDI
MEDTRONIC XOMED, INC.·00763000035211·PROSTHESIS 1133250 LIPPY CUP PSTN .6X4.0

Lippy

FDA UDI
MEDTRONIC XOMED, INC.·00681490034609·PROSTHESIS 1133250 LIPPY CUP PSTN .6X4.0

Starbond CoS

FDA UDI
S & S Scheftner GmbH·04260207850358·Ingots, 250g

Oticon

FDA UDI
Oticon A/S·05707131260154·RIA, BTE 13 WL 85 TC

Clear Readers

FDA UDI
Diversified Products, Inc.·00037741113362·

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

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

ADDplus

FDA UDI
Ulrich GmbH & Co. KG·04052536007301·Insert for screwdriver, for screw Ø 5.0 mm

CLYDESDALE PTC SPINAL SYSTEM

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

CPS DIRECT SL II SLITTABLE OUTER CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

EDWARDS LIFESCIENCES VANTEX CENTRAL VENOUS CATHETERS WITH THERMISTOR

FDA 510(k)
FDA Class 2 ·General Hospital

3 ML SYRINGE

FDA Adverse Event
Malfunction ·UNK·Product code FMI·October 14, 2025

DISPENSING PIN

FDA Adverse Event
Malfunction ·UNK·Product code KYX·October 14, 2025

CHARGING SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 20, 2013

L9000 LIGHTSOURCE

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·May 10, 2011

ONE TOUCH ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·August 21, 2008

M2A-MAGNUM MOD HD SZ 44MM 44MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024

MALLORY HEAD POR FMRL 13X170MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

M2A-MAGNUM PF CUP 50ODX44ID

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 3, 2024