31 results · 27ms · Sources: EU EUDAMED, US FDA

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0009613348-2024-010547

FDA Adverse Event
Injury ·INSTITUT STRAUMANN AG·Product code DZE·August 9, 2024

CHARGING SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 14, 2013

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·March 1, 2011

KIMBERLY-CLARK UNIVERSAL EXTREMITY DRAPE

FDA Adverse Event
Malfunction ·KIMBERLY-CLARK CORPORATION·Product code KKX·February 19, 2008

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

LOGIC TIBIA IMPLANT PSC INSERT, SZ 5, 13MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 13, 2023

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 17, 2024

LOGIC FEMORAL PS CEM LEFT SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·March 5, 2025

LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·June 30, 2022

LOGIC TIBIA IMPLANT PSC INSERT, SZ 3.5, 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

LOGIC TIBIA IMPLANT PSC INSERT, SZ 1, 13MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 26, 2023

OPTETRAK LOGIC

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 7, 2023

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 11, 2023

INSERT TIBIA LOGIC PSC SZ3 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·August 7, 2020

LOGIC TIBIA IMPLANT PSC INSERT, SZ 3, 13MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·July 30, 2024

LOGIC KNEE COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 11, 2023

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·November 8, 2024

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·June 26, 2023