33 results · 26ms · Sources: EU EUDAMED, US FDA

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TiWAVE-C™ Porous Titanium Cervical Cage

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526768451·GENUMEDI PSS GREEN I

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486002541·MCK Patellofemoral Component

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 29, 2018

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 29, 2018

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 28, 2018

Suzy Holemaker

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063771·

N/A

FDA UDI
Ortho Development Corporation·00822409128891·4-in-1 Cut Guide w/ Anterior Lip Size 1

SHELL CAGE, WAVE CAGE, LOOP CAGE

FDA 510(k)
FDA Class 2 ·Orthopedic

SWERV MAGNETOSTRICTIVE ULTRASONIC SCALER SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 28, 2019

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 19, 2022

SYRINGE 5ML LL BNS

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 29, 2021

IRRIGATION TUBING

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC·Product code GEI·January 16, 2015

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

ADVANTAGE SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013

CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·October 17, 2014

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 29, 2018

MK-2000

FDA Adverse Event
Injury ·NIDEK CO., LTD.·Product code HNO·November 14, 2019