8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TITANIUM ALLOY BONE SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780415046·Integra® Miltex® Nail Nipper, 4-5/8", Concave Jaws
EP-4 CLINICAL STIMULATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
RAPID-I KIT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SYNVISC
FDA Adverse Event
Injury
·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·June 19, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013
UNKNOWN DEPUY ASR HIP
FDA Adverse Event
Malfunction
·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 23, 2010
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
FDA Enforcement
Class II
·Terminated·Capintec Inc·April 1, 2020