51 results · 20ms · 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.

BIOFUSIONARY BEBE

FDA 510(k)
FDA Class 2 ·Physical Medicine

CoRoent

FDA UDI
Nuvasive, Inc.·00887517289087·CoRoent® Large MP, 11x9x23 12°

CHS

FDA UDI
Smith & Nephew, Inc.·03596010061966·AMBI COMPRESSION HIP SCREW PLATE 2SL 60MM 145D

Safesider HF

FDA UDI
ESSENTIAL DENTAL SYSTEMS, INC.·00766054002741·Safesider HF Intro Kit 21 mm

Drive

FDA UDI
Drive Devilbiss Healthcare·00822383729077·GrabBar,Chrome,12 inch,Knurled,3/cs,RTL

Rumex

FDA UDI
RUMEX INTERNATIONAL CORP.·00840159906743·Intraocular Needle Holder, 23 Ga, Tip Only

NEXFIN MODEL 2

FDA 510(k)
FDA Class 2 ·Cardiovascular

BACT/ALERT SN CULTURE BOTTLE

FDA 510(k)
FDA Class 1 ·Microbiology

Widex

FDA UDI
Widex A/S·05706069886139·WIDEX MOMENT MRB0 (Autumn Beige ) 220, RIC 10

Widex

FDA UDI
Widex A/S·05706069812374·Widex EVOKE E-PA (Autumn Beige ) 220, RC coil

EASYSPINE SCREW, UNKOWN SIZE OR TYPE

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·August 17, 2020

ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·March 5, 2019

POWERED PATIENT ROTATION BED

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code IKZ·May 20, 2013

MULTI-LINK RX VISION CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·August 14, 2008

TPS MICRO DRIVER

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HWE·May 4, 2011

ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE ROD, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020