8 results · 10ms · Sources: EU EUDAMED, US FDA

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Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case

FDA Recall
Terminated ·Cardinal Health 200, LLC·Product code KKK·July 28, 2017

CYSTOSCOPY PACK Ill (1) (2) CUSTOMED CONTENTS: (1) TABLE COVER REINFORCED 44" X 78" (2) TOWELS ABSORBENT 15" X 20" (2) LEGGINGS W/7" CUFF 30" X 42" (1) DRAPE CYSTOSCOPY T 60" X 87" 35" SMS STD (1) GOWN SURG.REINFORCED XL EXTRA LONG LEVEL IV Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

FDA Recall
Terminated ·Customed, Inc Calle Igualdad Final # 7·Product code KKK·May 20, 2014

GE Healthcare Innova X-ray Imaging Systems. The Digital Fluoroscopic Imaging System is indicated for use in diagnostic and interventional angiographic procedures of human anatomy. It is intended to replace image intensifier fluoroscopic systems in all diagnostic or interventional procedures. This device is not intended for mammography applications.

FDA Recall
Terminated ·GE Healthcare, LLC·Product code IZI·May 4, 2011

Ti-Magna Fx Washer Ti-Versa-FXII Femoral Fixation System S/C Plates The compression tube/plates of this trauma system are used with Ti-Versa-Fx II Femoral Fixation System lag screws for the internal fixation of proximal femoral and supracondylar fractures. The Ti-Magna Fx System is an osteosynthesis item for orthopedic use in open internal fixation of fractures of the femoral neck, condyle, or tibia, etc. The washer prevents the screw head from being buried in the bone.

FDA Recall
Terminated ·Zimmer, Inc.·Product code NDG·August 28, 2013

Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature

FDA Recall
Terminated ·Vital Signs Colorado Inc.·Product code KAK·August 17, 2012

Robotic hand accessory to InMotion Arm, rehabilitation robot.

FDA Recall
Terminated ·Interactive Motion Technologies, Inc.·Product code IKK·May 5, 2012

Cervical Extension Machine for Physical Therapy

FDA Recall
Terminated ·MedX Holdings, Inc.·Product code IKK·December 3, 2013

Kelyniam Custom Skull Implant (CSI), Model no. PEEK-IM1004

FDA Enforcement
Class II ·Terminated·Kelyniam Global, Inc.·May 23, 2018