19 results · 25ms · 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.

DISPOSABLE ARTHROSCOPY CANNULA SET

FDA 510(k)
FDA Class 1 ·Orthopedic

Trab. Punch

FDA UDI
KATENA PRODUCTS, INC.·00841668119969·Kelly Descemet's Punch

MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0130001·PLATE BENDER, UNIVERSAL

Ocata Anterior Cervical System

FDA UDI
Kalitec Direct LLC·B07308K0130000·Plate Bender Assembly

Flagship HS

FDA UDI
BRIVANT LIMITED·00816349010996·

UniTip Catheter

FDA UDI
Unisensor AG·07640172972083·

UniTip Catheter

FDA UDI
Unisensor AG·07640172971581·

UniTip Catheter

FDA UDI
Unisensor AG·07640172971598·

UniTip Catheter

FDA UDI
Unisensor AG·07640172972076·

ViperCath XC Peripheral Exchange Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDTRONIC INVISX BURR HOLE LOCK, MODEL 60520

FDA 510(k)
FDA Class 2 ·Neurology

TEGO CONNECTOR

FDA Adverse Event
Malfunction ·ICU MEDICAL, INC.·Product code FPA·September 19, 2014

NA

FDA UDI
Zimmer, Inc.·00889024024335·

VNGD CR TIB BRG 10X71/75

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 21, 2021

BIOMET CC I-BEAM TRAY 75MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 21, 2021

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 15, 2014

CAPSURE SP

FDA Adverse Event
Injury ·MPRI·Product code DTB·October 31, 2012

LIGAMAX-5MM ENDO CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code FZP·August 6, 2010

COBALT G-HV BONE CEMENT 40G

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 20, 2021