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

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Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO

FDA Enforcement
Class II ·Terminated·Clinical Innovations, LLC·February 4, 2015

The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or reduction of postpartum uterine bleeding.

FDA Enforcement
Class II ·Terminated·Clinical Innovations, LLC·October 21, 2015

Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates are intended for bone fixation such as: Arthrodesis of the 1st metatarsocuneiform joint to reposition and stabilize a metatarsus primus varus, Lisfranc arthrodesis, Mono or bi-cortical osteotomies or fractures near the 1st metatarsocuneiform joint.

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·August 8, 2012

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

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

EBI XFIX DFS Rail System (Adult Rail Gradual Swivel Clamp). The Biomet Rail System consists of a unilateral external fixator rail, modular bone screw clamps, and compression and distraction units. The device is used in the treatment of bone fractures.

FDA Enforcement
Class II ·Terminated·Biomet, Inc.·December 26, 2012

BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system

FDA Enforcement
Class II ·Terminated·Ebi, Llc·November 27, 2013

Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Drill/Awl Sleeve Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·December 31, 2014

Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178

FDA Enforcement
Class II ·Terminated·Ebi, Llc·December 26, 2012

Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusion device.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·October 9, 2013

Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·June 25, 2014

Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Polaris Spinal System is a non-cervical, pedicle screw spinal fixation device.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·March 27, 2013

Shortened Plug Driver; Low Volume Specialty Device; Qty:1; Rx Only; Non Sterile; Biomet Spine, Parsippany, NJ 07054 The Polaris Spinal Systems is a non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion as a pedical screw fixation system, a posterior hook and sacral/iliac screw fixation system, or as an anterior or anterolateral fixation system. Pedicle screw fixation is limited to skeletal mature patients for use with autograft and/or allograft. The device is indicated for all the following indications:degenerative disc disease (defined as discogeneic back pain with degeneration of the disk confirmed by history and radiographic studies), spondylolisthesis, and or lordosis) tumor, stenosis, pseudoarthrosis, or failed previous fusion

FDA Enforcement
Class II ·Terminated·Ebi, Llc·December 4, 2013

Cypher MIS Screw System-The system includes screws, various types and sizes of rods, and set screws. Various instruments are also available for use by the surgeon to facilitate implantation of the device. Non-cervical spinal fixation device intended for immobilization and stabilization as an adjunct to fusion.

FDA Enforcement
Class II ·Terminated·Ebi, Llc·January 14, 2015

Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal fixation device. 1)Screw Tower - REF 14-501660 2) Rod Reduce - REF 14-501661 3) Counter Torque - REF 14-501662

FDA Enforcement
Class II ·Terminated·Ebi, Llc·September 25, 2013