17 results · 21ms · 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.

Pressio 2 ICP Monitoring System

FDA 510(k)
FDA Class 2 ·Neurology

PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

FDA Adverse Event
Death ·SOPHYSA·Product code GWM·November 18, 2024

PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

FDA Adverse Event
Malfunction ·SOPHYSA·Product code GWM·November 18, 2024

PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

FDA Adverse Event
Malfunction ·SOPHYSA·Product code GWM·November 18, 2024

PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

FDA Adverse Event
Malfunction ·SOPHYSA·Product code GWM·November 18, 2024

DYNAMIC COMPRESSION SMA Staple System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902671814·STAPLE 8162108 8MM X 12MM 2PRONG SMA

LEONE SPA

FDA UDI
LEONE SPA·08033707093862·MICRO RAPID EXP.ONE-ARM EASY ACCESS 8 mm .

Peerless Buccal Tube

FDA UDI
ORMCO CORPORATION·00889989054125·PRLS 2NDMOL B/T 12DEG -27T 018 NDX LL

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221046055·Unitek(TM) Molar Band General Purpose Narrow Re...

CLICKFINE PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

COMCASET SAFETY IV CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital

ONE TOUCH BASIC ORIGINAL

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·March 22, 2002

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 12, 2011

ENDOVIVE TWO-PORT TTP JEJUNAL FEEDING TUBE CAP

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·June 11, 2013

SYNCHROMED EL

FDA Adverse Event
Injury ·RICE CREEK MANUFACTURING·Product code LKK·September 16, 2008

C-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·January 24, 2020

ONE TOUCH ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·May 5, 2010