Patent classifications
A61F9/007
LASER FIDUCIALS FOR AXIS ALIGNMENT IN CATARACT SURGERY
A fiducial is generated on an internal anatomical structure of the eye of a patient with a surgical laser. A toric artificial intraocular lens (IOL) is positioned so that a marker of the toric IOL is in a predetermined positional relationship relative to the fiducial. This positioning aligns the toric IOL with the astigmatic or other axis of the eye. The toric IOL is then implanted in the eye of the patient with high accuracy.
ADJUSTABLE FLOW GLAUCOMA SHUNTS AND ASSOCIATED SYSTEMS AND METHODS
The present technology is directed to adjustable shunts for treating glaucoma. In particular, some embodiments provide shunts having a plurality of individually actuatable flow control elements that can control the flow of fluid through associated ports and/or flow lumens. For example, each individually actuatable flow control element can be actuated to block and/or unblock a corresponding port and/or flow lumen. Accordingly, the shunts described herein can be manipulated into a variety of configurations that provide different drainage rates based on whether the ports and/or flow lumens are blocked or unblocked, therefore providing a titratable glaucoma therapy for draining aqueous from the anterior chamber of the eye.
FOLDING PRESSING-TYPE BALLOON STRUCTURE
A foldable pressing-type balloon structure (10), comprising a balloon body (100) used for arrangement in the Tenon capsule and a drainage component (200) capable of being closed automatically. The balloon body (100) is formed with a balloon cavity used for supplying normal saline or air; the balloon body (100) has a planar first surface (110) and a curved second surface (120); the height of the balloon body (100) along the first surface (110) is 0.2-2.0 cm; the drainage component (200) is connected to the second surface (120) of the balloon body (100) and communicated with the balloon cavity. The foldable pressing-type balloon structure (10) is implanted under the Tenon capsule, and a break is sealed by pressing by filling the inside of the balloon body (100) with a medium. Compared with scleral buckles in the prior art, fixing with buckles is not required, and it is only necessary to fix the position of the drainage component (200) by suturing to prevent displacement, so that an incision in surgery is reduced; moreover, because fixing with buckles is not required, extraocular muscles will not be pulled, so that a patient does not feel uncomfortable after surgery. The surgical method is simple in operation, the difficulty is reduced, and the time required for surgery is shortened.
FOLDING PRESSING-TYPE BALLOON STRUCTURE
A foldable pressing-type balloon structure (10), comprising a balloon body (100) used for arrangement in the Tenon capsule and a drainage component (200) capable of being closed automatically. The balloon body (100) is formed with a balloon cavity used for supplying normal saline or air; the balloon body (100) has a planar first surface (110) and a curved second surface (120); the height of the balloon body (100) along the first surface (110) is 0.2-2.0 cm; the drainage component (200) is connected to the second surface (120) of the balloon body (100) and communicated with the balloon cavity. The foldable pressing-type balloon structure (10) is implanted under the Tenon capsule, and a break is sealed by pressing by filling the inside of the balloon body (100) with a medium. Compared with scleral buckles in the prior art, fixing with buckles is not required, and it is only necessary to fix the position of the drainage component (200) by suturing to prevent displacement, so that an incision in surgery is reduced; moreover, because fixing with buckles is not required, extraocular muscles will not be pulled, so that a patient does not feel uncomfortable after surgery. The surgical method is simple in operation, the difficulty is reduced, and the time required for surgery is shortened.
Device for Controlled Injection Across a Variety of Material Properties
Described herein is a generalized injection device for delivering formulations of various mechanical properties to precise locations. Of particular interest is the manifestation intended for the application of a thermally responsive hydrogel to the tear duct for the purpose of occlusion, as a treatment for symptoms associated with dry eye syndrome. Further, a modular solution to the need for an injection device across a variety of applications, mechanism, and physical considerations is provided. This disclosure provides examples of methods for precise injection of low volumes, moisture retention in pre-filled injection devices, and actuation for automatic or manual injection, to name a few.
ROBOTIC ASSISTED SYSTEM FOR OPHTHALMIC SURGERY
The present invention discloses a robotic assisted system for ophthalmic surgery, comprising a first driving unit, a second driving unit and a third driving unit, wherein the three driving units can respectively complete the movement in three dimensions, the first driving unit is connected with the second driving unit, the second driving unit is connected with the third driving unit, and an instrument is arranged on the third driving unit; during operating, the third driving unit can drive the instrument assembly to move, the second driving unit can drive the third driving unit and instruments thereon to move, and the first driving unit can drive the second driving unit, the third driving unit on the second driving unit and the instruments on the third driving unit to move; the accurate control on the instruments can be completed by controlling the three different driving units. Through the specific RCM structure, the advantages of high precision and compact structure are achieved, and the present invention is suitable for various eye surgeries such as retinal bypass surgery, sub-retina injection and vitrectomy. The ophthalmic surgical device of the present invention has extremely high safety.
ROBOTIC ASSISTED SYSTEM FOR OPHTHALMIC SURGERY
The present invention discloses a robotic assisted system for ophthalmic surgery, comprising a first driving unit, a second driving unit and a third driving unit, wherein the three driving units can respectively complete the movement in three dimensions, the first driving unit is connected with the second driving unit, the second driving unit is connected with the third driving unit, and an instrument is arranged on the third driving unit; during operating, the third driving unit can drive the instrument assembly to move, the second driving unit can drive the third driving unit and instruments thereon to move, and the first driving unit can drive the second driving unit, the third driving unit on the second driving unit and the instruments on the third driving unit to move; the accurate control on the instruments can be completed by controlling the three different driving units. Through the specific RCM structure, the advantages of high precision and compact structure are achieved, and the present invention is suitable for various eye surgeries such as retinal bypass surgery, sub-retina injection and vitrectomy. The ophthalmic surgical device of the present invention has extremely high safety.
SURGICAL INSTRUMENT
A surgical blade (10) for being combined with an elongate handle (50) to form a cutting instrument for ophthalmic surgery includes a proximal portion (12) for being attached to the handle (12), an operative, distal portion (14), and a central portion (20) extending therebetween. The central portion (20) having a trapezoidal configuration that tapers radially inwardly from the proximal portion (12) to the distal portion and having a pair of sharpened lateral edges (21, 22). The distal portion (14) includes a first tapered section (23) defining a pair of sharpened lateral edges (24, 25) and extending from the central portion (20) to a substantially straight section (26) having a pair of sharpened lateral edges (27, 28). The substantially straight section (26) extends from the first tapered section (23) to a second tapered section (30) having a pair of sharpened lateral edges (32, 33) and terminating at a pointed tip (36).
Negative-pressure paracentesis syringe and use thereof
The present invention discloses a disposable negative-pressure anterior chamber Paracentesis syringe which belongs to the technical field of medical supplies. It comprises nine parts, including a needle cap, a Paracentesis syringe, a needle base, an internal needle, a protective cover of the internal needle, an airlock, a needle tube, a collection tube and a collection tube rack. The invention has the advantages that it fixes the Paracentesis syringe during puncture and limits the depth of the needle insertion, releases the aqueous humor slowly to prevent a sudden drop of the intraocular pressure, reduces the risk of the intraocular infection by separating the anterior chamber from outside and the collection tube can collect and store the aqueous humor directly.
Negative-pressure paracentesis syringe and use thereof
The present invention discloses a disposable negative-pressure anterior chamber Paracentesis syringe which belongs to the technical field of medical supplies. It comprises nine parts, including a needle cap, a Paracentesis syringe, a needle base, an internal needle, a protective cover of the internal needle, an airlock, a needle tube, a collection tube and a collection tube rack. The invention has the advantages that it fixes the Paracentesis syringe during puncture and limits the depth of the needle insertion, releases the aqueous humor slowly to prevent a sudden drop of the intraocular pressure, reduces the risk of the intraocular infection by separating the anterior chamber from outside and the collection tube can collect and store the aqueous humor directly.