26 results · 19ms · 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.

ACS LH2 IMMUNOASSAY

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

P.F.C. SIGMA

FDA UDI
DEPUY (IRELAND)·10603295240815·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING CURVED...

MODEL 3875 1 X 8 SC TEST STIMULATION LEAD

FDA 510(k)
FDA Class 2 ·Neurology

Airworks Nebulizer pe1200m

FDA 510(k)
FDA Class 2 ·Anesthesiology

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211346·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666153·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666160·

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211315·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666184·

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211353·

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211308·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666207·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666191·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024666177·

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211339·

NexGen® Legacy® Prolong®

FDA UDI
Zimmer, Inc.·00889024211322·

SCREW,FIXATION,BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·May 18, 2015

S8 ELITE - AMERICAS

FDA Adverse Event
Malfunction ·RESMED LTD.·Product code BZD·January 23, 2013

ARCHITECT HAVAB IGM REAGENT

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INT'L, LTD·Product code LOL·January 17, 2011

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 28, 2014