28 results · 28ms · Sources: EU EUDAMED, US FDA

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CAVEX ORTHOTRACE

FDA 510(k)
FDA Class 2 ·Dental

N/A

FDA UDI
GEORGE TIEMANN & CO.·B58212070·HOLDER, NEEDLE, GASTROENTEROLOGIC

PALACOS®

FDA UDI
Heraeus Medical GmbH·04260102135826·PALACOS® MV+G is indicated for use as bone ceme...

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm

LASER PERIPHERALS REUSABLE HOLMIUM FIBER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

STARLIGHT

FDA 510(k)
FDA Class 2 ·Neurology

EVIS EXERA III BRONCHOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·April 7, 2026

ATTAIN OTW

FDA Adverse Event
Injury ·MPRI·Product code LWP·April 10, 2013

ICEMAN THERAPY UNIT

FDA Adverse Event
Injury ·DJ ORTHOPEDICS DE MEXICO·Product code ILO·April 6, 2011

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·May 23, 2008

PERSONA ARTICULAR SURFACE MEDIAL CONGRUENT (MC)

FDA Adverse Event
Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·September 30, 2024

PERSONA ALL-POLY PATELLA

FDA Adverse Event
Injury ·ZIMMER MANUFACTURING B.V.·Product code MBH·September 30, 2024

PERSONA FEMUR CEMENTED CRUCIATE RETAINING (CR)

FDA Adverse Event
Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·September 30, 2024

PERSONA CEMENTED TIBIA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 30, 2024

OPTETRAK HI-FLEX TIBIAL INSERT SZ 3 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 27, 2024

TIBIA CEMENTED 5 DEGREE STEMMED RIGHT SIZE C

FDA Adverse Event
Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·June 3, 2025

ALL-POLY PATELLA CEMENTED 29 MM DIAMETER

FDA Adverse Event
Injury ·ZIMMER MANUFACTURING B.V.·Product code MBH·June 3, 2025

FEMUR CEMENTED (CR) STANDARD NITRIDED RIGHT SIZE 7

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 3, 2025

ARTICULAR SURFACE (MC) RIGHT 10 MM HEIGHT

FDA Adverse Event
Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·June 3, 2025

ACTIVA

FDA Adverse Event
Malfunction ·MPRI·Product code MHY·June 28, 2021