34 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.

EPI-DERM SILICONE GEL SHEETING

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Leksell Stereotactic System

FDA UDI
Elekta Instrument AB·07340048308069·POST CURVED

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·40677964024588·The ENDO CARRY-ON Procedure Kit contains all of...

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169347847·TEMPLATE 3003948 ZEVO 48MM 3 LVL

SCANLAN® Legacy Micro Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159032956·Legacy FRP FH 1MM DD PF RT 10"

OLYMPUS ENDOSCOPIC FLUSHING PUMP MODEL OFP-1

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

UCSS SCREW SET

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MRW·June 4, 2009

UCSS SCREW SET

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code HWC·June 4, 2009

OT BASIC METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 8, 2010

HF SENSOR DELIVERY SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.·Product code MOM·February 12, 2020

OT BASIC METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 6, 2011

PDS LL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code NEW·March 14, 2013

TMJ CONCEPTS

FDA Adverse Event
Injury ·TMJ CONCEPTS·Product code LZD·February 23, 2011

GEMSTAR

FDA Adverse Event
Malfunction ·HOSPIRA GLOBAL MEDICAL AFFAIRS·Product code FPA·January 30, 2008

OT BASIC ENHANCED METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 6, 2011

UCSS

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 2, 2016

OT BASIC METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 4, 2011

OT BASIC ENHANCED METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 12, 2011

UCSS SCREW SET

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·January 3, 2011