25 results · 23ms · Sources: EU EUDAMED, US FDA

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Piccolo Composite Nailing System

FDA 510(k)
FDA Class 2 ·Orthopedic

XENMATRIX

FDA UDI
Davol Inc.·00801741074219·XenMatrix AB Surgical Graft, 10 cm x 10 cm

RUSCH

FDA UDI
TELEFLEX INCORPORATED·14026704630766·Rusch Polaris FO Blade, Miller 1, Sterile

Pro Advantage

FDA UDI
NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P1510103·PA TAPE SURGICAL PAPER 1X10YD 12/BX 12BX/CS - (CS)

BrightGear Headgear

FDA UDI
ORMCO CORPORATION·00889989059854·HI-PULL UNIT MED/BLACK

Mini-Mono®

FDA UDI
Forestadent Bernhard Förster GmbH·EFORN74101510101·Mini-Mono-Bracket Roth 'N' .022" max. 1 right

Mini-Mono®

FDA UDI
Forestadent Bernhard Förster GmbH·EFORO74001510101·Mini-Mono-Bracket Roth 'N' .022" max. 1 left

FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL: KD-5963NU, KD-5008

FDA 510(k)
FDA Class 2 ·Cardiovascular

SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70

FDA 510(k)
FDA Class 2 ·Dental

INTELLIS

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·April 19, 2018

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code IOR·June 6, 2013

STANDARD INSERT

FDA Adverse Event
Injury ·DEPUY INTL, LTD.·Product code KWA·June 29, 2011

LIFESHIELD CONNECTOR

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code GCE·August 28, 2008

LATITUDE ELBOW ANATOMIC HUMERAL SPOOL SZ PETIT+ SIDE DROIT

FDA Adverse Event
Injury ·TORNIER INC·Product code JDB·September 20, 2024

AGC MOD TIB I DCM BRNG 16X75

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 19, 2018

AGC MOD TIB II POR PLATE 75

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·November 19, 2018

M2A-MAGNUM 42-50MM TPR INSRT-6

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 15, 2019

TAPERLOC POR FMRL LAT 7.5X135

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 15, 2019

M2A-MAGNUM MOD HD SZ 44MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 15, 2019

LIFE SCOPE G9

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 13, 2024