28 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.

Solus Gold Embolization Device

FDA 510(k)
FDA Class 2 ·Cardiovascular

TempoCemID

FDA UDI
DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG2132000·Temporary cement smartmix system. Invisible und...

Bellinger

FDA UDI
Bellinger A/S·05712544166955·Spectacle frame

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702827323·ELVAREX 3/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0132000·Rod Reducer, Axial, NIDO

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221049100·Unitek(TM) Permachrome Resilient Stainless Stee...

RENMED CONTAMI-SHIELD BREATHING CIRCUIT SLEEVE, MODEL 9999/01

FDA 510(k)
FDA Class 2 ·Anesthesiology

VITEK 2 AST-GN PIPERACILLIN/TAZOBACTAM

FDA 510(k)
FDA Class 2 ·Microbiology

FASTTAKE

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·January 16, 2002

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124305·CR Femoral Trial Sz 2 R

InSitu Hip System

FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127022449·Femoral Head, 32mm, -4mm, Biolox

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523148042·PS Femoral Trial Sz 2 R

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143177·R PS Cemented Femoral Component Sz 2

BD DIFCO¿ POTATO DEXTROSE AGAR

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code JSG·May 17, 2024

Truliant

FDA UDI
Exactech, Inc.·10885862595911·

ENSITE CLASSIC SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code DQK·February 9, 2010

RECOVERY FILTER SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 22, 2008

ASR ACETABULAR CUPS 60

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 12, 2011

GYNECARE GYNEMESH* PS

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTO·July 9, 2013

G7 LONGEVITY NEUTRAL 36MM F

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 1, 2024