17 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CodMan Certas Plus Programmable Valve
FDA 510(k)
FDA Class 2
·Neurology
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269828·
AVANOS
FDA UDI
Avanos Medical, Inc.·00193493934560·AVANOS* Single-Shot Epidural Trays
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1822650·18mm H x 22mm W x 65mm L x 0 degrees XLIF
Halyard
FDA UDI
Avanos Medical, Inc.·10680651934564·HYH,EP TRY,S-SHOT,-,-,10
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122292·Kwire .070X9" (1.8x225mm)
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X182265120·18mm H x 22mm W x 65mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18226580·18mm H x 22mm W x 65mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L182265120·18mm H x 22mm W x 65mm L XLIF Trial 12 degree L...
LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VIALOK SINGLE VIAL ACCESS DEVICE VENTED
FDA 510(k)
FDA Class 2
·General Hospital
TUBE SET FOR SUCTION SINGLE-USE
FDA Adverse Event
Malfunction
·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·December 2, 2019
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013
CONTINUUM TRILOGY PROVISIONAL LOCKING SCREW
FDA Adverse Event
Malfunction
·ZIMMER INC·Product code LXH·July 12, 2011
HEARTSTART MRX AIRWORTHY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 4, 2014
BD NEXIVA DUAL PORT 20GA 1.00IN (1.1 MM X 25 MM)
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 6, 2019
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
FDA Enforcement
Class II
·Terminated·Kimberly-Clark Corporation·December 25, 2013