1,370 results
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17ms
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Sources: EU EUDAMED, US FDA
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Genesis Screw-In Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Genesis Dual Thread Screw-In Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Genesys spine, Binary Screwdriver, GCP221, component of the Binary Anterior Cervical Plating System The Genesys Spine Binary Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine. It is to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to C7). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), spondylolisthesis, trauma (i.e. fractures or dislocations), tumors, deformity (defined as kyphosis, lordosis, or scoliosis),pseudoarthrosis, failed previous fusion, and/or spinal stenosis.
FDA Recall
Terminated
·Genesys Orthopedics Systems, LLC
1250 S Capital of Texas Hwy Ste 600
Bldg # 3
West Lake Hills TX 78746-6446·Product code LRZ·November 5, 2015
AlternatiV+ Max Knotless Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Fixone Biocomposite Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Genesis Push-In Suture Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Genesis Knotless Anchor
FDA Recall
Open, Classified
·Aju Pharm Co., Ltd.
Room 201, Room 207, Bl A
Bundangtekeunopakeu; 697 Pangyo-Ro; Bundang
Seongnam Korea (the Republic of)·Product code MAI·December 17, 2025
Non-ablative Fractional Laser Systems, Model: WFB-01
FDA Recall
Open, Classified
·WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China·Product code ONG·August 23, 2024
Diode Laser Hair Removal model: WLA-01
FDA Recall
Open, Classified
·WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China·Product code GEX·August 23, 2024
Portable X-ray system
FDA Recall
Open, Classified
·DIGIMED CO., LTD
401, 402, 406~411-ho, A-dong 101, Gasan digital 2-ro, Geumcheon-Gu
Seoul Korea (the Republic of)·Product code EHD·June 19, 2025