2,010 results · 23ms · Sources: EU EUDAMED, US FDA

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ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580207·Rod(CoCr), Ø6.0 x 200mm

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981246679·Interbody, 39mm x 30mm X 20mm, 20 Deg

Meridian

FDA UDI
Seaspine Orthopedics Corporation·10889981265922·Trial, 39mm x 30mm x 20mm, 20 deg

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321320200·

51CM(20.1INCH) TFT MONOCHROME LCD MONITOR, MU5111BW

FDA 510(k)
FDA Class 2 ·Radiology

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023692·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023678·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023722·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023685·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023654·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023661·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023715·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361023708·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

SIMPULSE SOLO

FDA Adverse Event
Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FQH·April 30, 2013

ENCORE SYSTEM

FDA Adverse Event
Injury ·SIESTA MEDICAL INC.·Product code ORY·September 24, 2014

ASKU

FDA Adverse Event
Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

COCHLEAR OSIA OSI200 IMPLANT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MCM·July 12, 2020

AMS INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·April 25, 2019