MEDICAL DEVICE REMOVAL

Brand Owner (click to sort) Address Description
ACUTREAT MSD CONSUMER CARE, INC. 3030 Jackson Avenue Memphis TN 38151 Medical device for the removal of warts, corns, and calluses;
AURORA James R. Rynerson 1200 Talon Way Franklin TN 37069 medical device for the removal of biofilm from the eyelid;
CALCULA Calcula Technologies, Inc. 959 Peralta Avenue San Francisco CA 94110 Medical device for the removal of kidney stones from the human body and the treatment of other urological diseases and therapies consisting of catheters and parts and fittings therefor; an imaging system consisting of fiber optic camera and memory module, and parts and fittings therefor, all for medical purposes;
FREEZE OFF MEDTECH PRODUCTS INC. Suite 250 660 White Plains Road Tarrytown NY 10591 Medical device for the removal of warts;
MASKIN MEIBUM EXPRESSOR MGD INNOVATIONS, INC. 3001 Swann Avenue Tampa FL 33609 Medical device for removal of secretion from oil glands;MEIBUM EXPRESSOR;
MOLLI RE.MARKABLE MOLLI Surgical Inc. Suite 400 50 Wellington St. East Toronto, ON M5E1C8 Canada medical device for the removal of magnetized localization markers;
VERSATA Neurovasc Technologies Inc. 3 Jenner, Suite 100 Irvine CA 92618 Medical device for removal of clots in the treatment of ischemic stroke;
VERSI-SR Neurovasc Technologies Inc. 3 Jenner, Suite 100 Irvine CA 92618 Medical device for removal of clots in the treatment of ischemic stroke;
VERSISR Neurovasc Technologies Inc. 3 Jenner, Suite 100 Irvine CA 92618 Medical device for removal of clots in the treatment of ischemic stroke;
 

Where the owner name is not linked, that owner no longer owns the brand

   
Technical Examples
  1. This document describes, among other things, a method of operating a medical device comprising updating a regulatory approval status stored in at least one of the medical device or a second device operable to communicate with the medical device, and enabling or disabling the at least one function in the medical device based on the regulatory approval status. The regulatory approval status corresponds to at least one function performable by the medical device.