12 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ARC-600
FDA 510(k)
FDA Class 2
·Radiology
SMALL BONE EXTERNAL FIXATION SYSTEM CASE
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665032185·
SeaSpine Spacer System - Pacifica™
FDA UDI
Seaspine Orthopedics Corporation·10889910058670·Pacifica Trial, 9mm x 20mm x 7mm
SeaSpine Spacer System - Pacifica™
FDA UDI
Seaspine Orthopedics Corporation·10889981058678·Pacifica Trial, 9mm x 20mm x 7mm
CAREFINE PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
TAIWAN KING STRONG POWERED WHEELCHAIR, TP 01
FDA 510(k)
FDA Class 2
·Physical Medicine
G7 BISPHERICAL SHELL 52E
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWZ·March 12, 2019
MEDTRONIC
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LWS·May 30, 1997
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·January 29, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code FNL·December 13, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2014
Comprehensive HHR Tess Cleat, Item Nos. 110260 110261 110262 110263 Product Usage: N/A
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·December 4, 2019