24 results · 23ms · 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.

Kalera Vacuum Aspiration Catheter (K-VAC)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Intraoral Scan Body

FDA UDI
RP - CONEXOES RESTAURADORAS LTDA·07901059074994·

GORNEY SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896098404·GORNEY SCISSORS STRAIGHT BLADE POWER CUT GOLD

Reamer

FDA UDI
Treace Medical Concepts, Inc.·00810111225601·Barrel Reamer

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

FDA 510(k)
FDA Class 1 ·General Hospital

V SET

FDA 510(k)
FDA Class 2 ·General Hospital

ANSPACH CONSOLE - 200419

FDA Adverse Event
Malfunction ·BLUE BELT TECHNOLOGIES·Product code HBE·April 23, 2020

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·July 9, 2019

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·July 9, 2019

ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY AG·Product code MTA·October 24, 2014

ACS MULTI-LINK CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MAF·August 11, 2011

DEPUY ASR XL FEM IMP SIZE 43

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KXA·July 1, 2013

UNKNOWN DEEP BRAIN NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 16, 2016

NEEDLE 18GA 1-1/2IN SB TW

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·August 5, 2020

NAVIO SURGICAL SYSTEM INDIA

FDA Adverse Event
Injury ·BLUE BELT TECHNOLOGIES·Product code OLO·December 2, 2020

UNKNOWN HIP FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWY·November 20, 2019

UNKNOWN HIP FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 20, 2019

UNKNOWN HIP FEMORAL STEM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 20, 2019

UNKNOWN HIP FEMORAL STEM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 20, 2019

PROXIMATE*HCS HEMORR CIR STAPL

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 22, 2019