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

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OPTETRAK LOGIC COMBINATION TIBIAL TRAY

FDA 510(k)
FDA Class 2 ·Orthopedic

LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

LOGIC FEMORAL PS CEM RIGHT SZ 2

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024

OPTETRAK HI-FLEX TIBIAL INSERT SZ 4 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·August 25, 2022

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964072802·Endo Carry-On Procedure Kit

Tasso+ Convenience Kit

FDA UDI
Tasso Inc.·00850038691011·

Disposable Blade

FDA UDI
KATENA PRODUCTS, INC.·00841668113196·BARD-PARKER BLADE #11 PACK OF 50

MHS 5000

FDA 510(k)
FDA Class 1 ·Obstetrics/Gynecology

DIASTAT ANTI-CARDIOLIPIN IGA, MODEL FCAR 500

FDA 510(k)
FDA Class 2 ·Immunology

PUMP, INFUSION

FDA Adverse Event
Injury ·NULL·Product code FRN·April 19, 2022

AS VEGA PS TIBIAL PLATEAU CEMENTED T3

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 4, 2018

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 3, 2022

7900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 3, 2013

ALTRX NEUT 36IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 19, 2014

9600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

AS COLUMBUS REV F FEMUR CEMENTED F5L

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS VEGA PS TIBIAL PLATEAU CEMENTED T3+

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS VEGA PS TIBIAL PLATEAU CEMENTED T2

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

AS COLUMBUS REV F TIB.OFFSET CEMENT.T5

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 249 cm, REF 3688UK, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702

FDA Enforcement
Class II ·Terminated·Ecolab Inc·February 19, 2014