45 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.

FUJIFILM Ultrasonic Processor SP-900 and FUJIFILM Ultrasonic Probe PB2020-M

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

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813872·GENUMEDI PRO SILVER SIZE VII

LuxaPrint Ortho 385

FDA UDI
DMG Chemisch-Pharmazeutische Fabrik GmbH·EMDG1712070·(Meth) acrylate-based light-curing resin exclus...

LuxaPrint Ortho 385

FDA UDI
DMG Digital Enterprises SE·D9821712070·(Meth) acrylate-based light-curing resin for th...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292992·

Key Surgical K-Wires and Steinmann Pins

FDA UDI
KEY SURGICAL, INC.·00849771012757·K-Wires, Double diamond, .045-inch (1.1mm) diam...

NA

FDA UDI
KEY SURGICAL, INC.·10849771049378·K-Wires, Double diamond, .045-inch (1.1mm) diam...

9300

FDA UDI
HANS RUDOLPH, INC.·00817136022000·FILTER/REG/GAGE LOWPRESS 25PSI

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383549660·Gutta Percha Points is used to root canal filin...

VACUTRON

FDA UDI
Allied Medical, LLC·00026072009970·

NEODENT IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

MASTER GUARD NITRILE BLUE POWDERED EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

VACUTRON

FDA UDI
Allied Medical, LLC·00026072009987·

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·June 14, 2013

COULTER AC-T DIFF 2 ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 1, 2011

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 22, 2008

VITALITY SCREW, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

VITALITY SCREW, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

VITALITY SCREW, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

VITALITY SCREW, UNKNOWN SIZE OR TYPE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019