Ears, Nose, and Throat Extractor
    61.
    发明申请

    公开(公告)号:US20210346043A1

    公开(公告)日:2021-11-11

    申请号:US17315098

    申请日:2021-05-07

    Applicant: Veartech, Inc.

    Abstract: There is disclosed in one example an apparatus for extracting a foreign body (FB) from a bodily orifice, including: a connector having a receiver to pneumatically seal to a suction source; a hollow shaft pneumatically coupled to the connector; a hollow tip pneumatically coupled to the hollow shaft; and a valve disposed between the hollow tip and the connector, wherein the valve is biased to an open position, and the valve, when closed pneumatically isolates the hollow tip from the connector, and when open allows a continuous air flow passage between the connector and the hollow tip; and means to release the valve, whereby the valve opens when the means are activated.

    Nose clearing assembly
    63.
    发明授权

    公开(公告)号:US11160574B2

    公开(公告)日:2021-11-02

    申请号:US16728110

    申请日:2019-12-27

    Applicant: Dave Contreras

    Inventor: Dave Contreras

    Abstract: A nose clearing assembly for cleaning a user's nostrils includes a tube that is insertable into a nostril of user. A swab is coupled to the tube and the swab can be inserted into the user's nostril. The swab is comprised of a fluid absorbent material for absorbing fluid mucous from the user's nostril. A shovel is coupled to the tube and the shovel can be inserted into the user's nostril. The shovel lies on a plane that is oriented perpendicular to a longitudinal axis of the tube. In this way the shovel can engage, and subsequently remove, dried mucous from the user's nostril.

    IMPLANTABLE DEVICE
    65.
    发明申请

    公开(公告)号:US20210330316A1

    公开(公告)日:2021-10-28

    申请号:US17356381

    申请日:2021-06-23

    Abstract: An implantable device for aiding in generating connective tissue between a pair of anatomical structures in a mammalian body is provided. The device includes an elongate, flexible tether which can be secured between the anatomical structures and which carries a scaffold which is generally porous so as to be capable of promoting tissue ingrowth and collagen deposition along its length. The scaffold extends along the tether for a sufficient distance so that it is securable in at least close proximity to an anatomical structure at either end. The pores in the scaffold extend through the scaffold and each has a diameter in the range of about 10 μm to about 200 μm. The length of the tether is selected to be a desirable maximum distance between the anatomical structures along a desired path when secured therebetween.

    BALLOON CATHETER INFLATION APPARATUS AND METHODS

    公开(公告)号:US20210322734A1

    公开(公告)日:2021-10-21

    申请号:US17205912

    申请日:2021-03-18

    Abstract: An inflation device includes a syringe body containing a bore. The bore holds a fluid that is used to inflate a separate device such as a dilation balloon. A plunger assembly slides within the syringe bore and contains a sealing member that forms a fluid tight seal with the syringe body. A shut-off valve is disposed within the distal end of the syringe body. The distal end of the syringe body has a fluid bypass channel fluidically coupled to the aperture of a connector. The shut-off valve has a spring-biased moveable piston with a bypass lumen contained therein, wherein the bypass lumen forms a fluid path between the bore and the fluid bypass channel when the pressure of the fluid is below a threshold value. The fluid path between the bore and the fluid bypass channel is interrupted when the pressure of the fluid is above the threshold value.

    Sinus dilation catheter
    67.
    发明授权

    公开(公告)号:US11147908B2

    公开(公告)日:2021-10-19

    申请号:US16393594

    申请日:2019-04-24

    Abstract: A balloon dilation catheter includes a substantially rigid inner guide member and a movable shaft coupled to a balloon that is slidably mounted on the substantially rigid inner guide member. To treat a sinus cavity of a subject using the balloon dilation the substantially rigid inner guide member is advanced into a drainage pathway of the sinus (e.g., frontal recess or maxillary sinus) of the subject via a nasal passageway. The shaft and balloon are advanced in a distal direction over the substantially rigid inner guide member to place the balloon in the drainage pathway. The balloon is inflated to expand or otherwise remodel the drainage pathway.

    Laryngoscope Blade And Method For Producing A Laryngoscope Blade

    公开(公告)号:US20210307600A1

    公开(公告)日:2021-10-07

    申请号:US17350774

    申请日:2021-06-17

    Inventor: Bernd Krause

    Abstract: A method for producing a laryngoscope blade and a laryngoscope blade including a base blade and a tube which is arranged at least in part on an outer face of the base blade, extends approximately in a longitudinal direction of the base blade and is firmly connected to the base blade, wherein the tube, at its side facing toward the base blade, has at least in part a longitudinally extending corrugation which, with the outer face of the base blade, forms a longitudinally extending cavity, wherein the tube is connected to the base blade by a respective soldering seam in the lateral edge regions of the corrugation.

    Devices And Methods For Treating A Lateral Surface Of A Nasal Cavity

    公开(公告)号:US20210244458A1

    公开(公告)日:2021-08-12

    申请号:US17242727

    申请日:2021-04-28

    Applicant: Arrinex, Inc.

    Abstract: The invention disclosed here generally relates to devices that can modify a property of a nerve. Specifically, the subject invention is contemplated to modify the posterior nasal nerve signal conduction in such a way so as to reduce the signals transmitted to the nasal cavity. Reduction or interruption of the nerve signals results in the reduction of the distal organ activity. In particular, embodiments of the present invention allow for increased lateral contact or apposition of the target tissue region having at least one posterior nasal nerve with the end effector surface by lateral and/or longitudinal translation of the end effector relative to the surgical probe shaft. This improved lateral surface contact has several benefits, including improved patient outcomes and patient safety as the end effector is adequately in contact with target tissue for subsequent ablation therapy.

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