9,382 results · 60ms · Sources: EU EUDAMED, US FDA

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ARTHREX INC.

FDA Adverse Event
Injury ·ARTHREX INC.·Product code HRY·July 30, 1998

ARTHREX, INC

FDA Adverse Event
Injury ·ARTHREX, INC·Product code HTN·November 13, 2007

ARTHREX, INC.

FDA Adverse Event
Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·September 5, 2013

ARTHREX, INC

FDA Adverse Event
Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·March 13, 2015

ACL TIGHTROPE RT- ARTHREX INC.

FDA Adverse Event
Injury ·ARTHREX·Product code HTY·January 21, 2016

OSFERION

FDA Adverse Event
Injury ·OSFERIONBIOMATERIALS CORP. MISHIMA FACTORY·Product code MQV·April 28, 2026

OSFERION

FDA Adverse Event
Injury ·OSFERIONBIOMATERIALS CORP. MISHIMA FACTORY·Product code MQV·April 28, 2026

LOW PROFILE LAPIDUS PLATE, TITANIUM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRS·June 12, 2024

SUPERMX COMPRESSION STAPLE, 20W X 20L

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code JDR·June 3, 2024

RETROSCREW 9 X 20 MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MAI·January 17, 2006

CCU, ARTHREX SYNERGY UHD4

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code GCJ·March 21, 2024

UNK

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HSB·June 10, 2024

APSII CONTROL CONSOLE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWE·February 14, 2024

ALLOSYNC¿ CB DBM PUTTY, 10CC

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MQV·May 21, 2024

SUPERMX NITI STAPLE W/ INSTRS, 20W X 20L

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code JDR·May 22, 2024

UNK

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HWC·February 27, 2026

ARTHREX INC PEEK TENODESIS SCREW WITH DISPOSABLE SHEATH 7X20MM

FDA Adverse Event
Injury ·ARTHREX MANUFACTURING INC.·Product code MAI·March 1, 2024

FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code GAT·June 6, 2024

FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code GAT·June 18, 2024

ACL REPAIR TIGHTROPE, WITH INTERNALBRACE

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MBI·June 18, 2024