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BioHorizons 0.050 Hex Driver, Regular, REF 300-350, BioHorizons Implant Systems, Inc., Birmingham, AL 35243, non-sterile, Rx only

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·March 12, 2007

Allen Medical C-Flex, Polar Head Positioner Catalog Number: A-70700-A1 Product is a medical device used to maintain the position of an anesthetized patient during surgery.

FDA Recall
Terminated ·Allen Medical Systems, Inc. One Post Office Square·Product code CCX·November 27, 2007

The Maestro System 204-503, Straight Permucosal Ext, 5mm x 3mm

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code NDP·June 3, 2005

BioHorizons 0.050 Hex Driver, Long, REF 300-351, BioHorizons Implant Systems, Inc., Birmingham, AL 35243, non-sterile, Rx only

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·March 12, 2007

Biohorizons 3.0mm Overdenture Implant System, REF 30120S2, (3 mm x12 mm-2mm collar), Biohorizons Implant Systems, Inc., Birmingham, AL 35243

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·April 18, 2007

Allen Traction Boot, Modular, OT 1000 Traction Device Boot Assembly, Fracture Table Orthopedic Leg Holders, non-invasive medical devices designed to attach to orthopedic fracture tables to aid clinical staff in applying traction to the leg of a patient during surgical procedures.

FDA Recall
Terminated ·Allen Medical Systems, Inc. One Post Office Square·Product code HST·February 28, 2013

BioHorizons 0.050 Hex Driver, Regular, REF 134-350, BioHorizons Implant Systems, Inc., Birmingham, AL 35243, non-sterile, Rx only. The product is part of a Prosthetic Instrumentation system Kit 51-K , Manufactured by Innovision, Inc., and the kits are assembled by BioHorizons.

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·March 12, 2007

BioHorizons Maximus 3.0 surgical kit, also marketed as BioHorizons One-piece 3.0 Implants and Surgical Kit

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·December 28, 2005

Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder Positioner is intended to allow for the controlled manipulation of the arm and shoulder joint during arthroscopic surgical procedures.

FDA Recall
Terminated ·Allen Medical Systems, Inc. One Post Office Square·Product code HST·January 3, 2017

Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.

FDA Recall
Terminated ·Allen Medical Systems, Inc. One Post Office Square·Product code HST·November 23, 2016

Allen C-Flex Head Positioning System non-invasive medical device used to support a patient's head during spine surgery Catalog Numbers: A-70700 and A-70701-2

FDA Recall
Terminated ·Allen Medical Systems, Inc. One Post Office Square·Product code CCX·November 16, 2011

BioHorizons 0.035 Hex Driver, REF 300-377, BioHorizons Implant Systems, Inc., Birmingham, AL 35243, non-sterile, Rx only, REF 300-377.

FDA Recall
Terminated ·BioHorizons Implant Systems Inc One Perimeter Park South·Product code DZE·March 12, 2007

SOUTHERN IMPLANTS REF IBR12d-13, Implant, Ext. Hex, tapered 12o Co-Axis(TM) intended for surgical placement in the upper or lower jaw to provide a means for prosthetic attachment of crowns, bridges or overdentures utilizing delayed or immediate loading.

FDA Recall
Terminated ·Southern Implants, (Pty.) Ltd. One Albert Road Irene, Gauteng South Africa·Product code NHA·March 8, 2018

MHI-TM2000 Linear Accelerator System Product Usage: MHI-TM2000 Linear Accelerator System is intended for radiation therapy of lesions, tumors and conditions anywhere in the body where radiation treatment is indicated.

FDA Recall
Terminated ·Hitachi Ltd., Medical System Operations Group 2-1 Shintoyofuta Kashiwa Japan·Product code IYE·December 8, 2017

Allen Medical Systems PAL Pro Stirrups Catalog Number: A-10051-A1

FDA Recall
Terminated ·The OR Group, Inc. A Subsidiary of Hill-Rom Inc. One Post Office Square·Product code FWZ·June 2, 2003

Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperthermic Perfusion System intended to raise the temperature of the thoracic or peritoneal cavity to a target temperature.

FDA Recall
Terminated ·Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands·Product code LGZ·June 4, 2021