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LOCK DEVICES

FDA UDI
Alps South, LLC·00713980001355·Gear (Pinion Shaft)

Construct ™

FDA UDI
Ascension Orthopedics, Inc.·10381780245940·Construct® Ankle Fusion Plate System The locki...

Total Foot System 2

FDA UDI
Smith & Nephew, Inc.·00885556839805·1.8MM LOCKING DRILL GUIDE (BLUE)

Construct ™

FDA UDI
Ascension Orthopedics, Inc.·10381780245933·Construct® Ankle Fusion Plate System The locki...

Proximal Humeral Fracture Plate System

FDA UDI
Smith & Nephew, Inc.·00885556829929·1.9MM LOCKING DRILL GUIDE

Surgical Instruments

FDA UDI
Smith & Nephew, Inc.·00885556829936·2.4MM LOCKING DRILL GUIDE

Total Foot System 2

FDA UDI
Smith & Nephew, Inc.·00885556839812·2.5MM LOCKING DRILL GUIDE (YELLOW)

METASUL LDG

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·November 11, 2010

Integra®

FDA UDI
Ascension Orthopedics, Inc.·10381780245957·Integra®Total Foot System The locking drill gui...

Integra®

FDA UDI
Ascension Orthopedics, Inc.·10381780245964·Integra®Total Foot System The locking drill gui...

ECHELON FLEX 60 POWERED PLUS ENDOPATH STAPLER ARTICULATING ENDOSCOPIC LINEAR CUT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 11, 2019

BLAKE DRAIN UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GBX·March 1, 2018

JVAC UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code JOL·March 1, 2018

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2021

ECHELON ENDOPATH STAPLER

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 5, 2021

CD004, 12/15MM RETRIEVAL SYSTEM, 5/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·July 3, 2024

LIGAMAX-5MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 31, 2010

LIGAMAX-5MM ENDO CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 22, 2018

TRI-STAPLE 2.0

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·July 22, 2024

THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 22, 2023