Medical devices and methods of treating subjects using such medical devices are described. The medical device may include a housing with at least two chambers including a first chamber adjacent to a second chamber; a barrier between the first chamber and the second chamber; and a soft, flexible base. The first and second chambers may be airtight, the barrier configured to establish fluid communication between the first chamber and the second chamber upon an application of force to the barrier.

An apparatus for dispensing eye drops can comprise a housing that defines a receptacle. The receptacle can be configured to receive a cartridge having a solution therein. An actuator can be movable between a first position and a second position. The actuator can be positioned with respect to the receptacle so that, when the cartridge is received in the receptacle and the actuator is moved from the first position to the second position, the actuator deforms the cartridge by a select amount to dispense a predetermined quantity of solution from the cartridge.

For allowing an access to an eye during a rinsing process it is suggested to configure an eye opening device in such a way that the eye opening device comprises two wing-like spreading elements for pulling the upper eyelid and the lower eyelid of the eye apart so as to support the opening of the eye during a rinsing process, wherein two access gaps are formed laterally between the two wing-like spreading elements of the eye opening device.

Configurations are disclosed for a health system to be used in various healthcare applications, e.g., for patient diagnostics, monitoring, and/or therapy. The health system may comprise a light generation module to transmit light or an image to a user, one or more sensors to detect a physiological parameter of the user's body, including their eyes, and processing circuitry to analyze an input received in response to the presented images to determine one or more health conditions or defects.

An ophthalmological device for the treatment of keratoconus includes a cylindrical reservoir made of a non-conductive material, open at the top and bottom, and formed by two telescopically engaged portions, a lower one open at the bottom and connected to a cylindrical chamber of smaller diameter, also open at the bottom and formed by an external annular chamber that is concentrically arranged around the chamber and is closed at the top, open at the bottom, and adapted to be placed on the eye; a first metallic conductor, housed in the container and connected to a terminal of a DC voltage generator, to the other terminal of which a second metallic conductor is connected; a first conduit provided with a closing device, one end of the first conduit flowing into the annular reservoir, the other end being located externally thereto, whereby vacuum may be applied through the first conduit; and a second conduit provided with a closing device, one end of the second conduit passing through the annular reservoir at its lower edge and flowing into the container, the other end being located externally to the annular reservoir. During irradiation, a hydrating solution is administered from above through the metallic conductor that touches the eye and is released through the conduit to avoid the excessive absorption of incident energy by the hydrating solution while maintaining a minimum thickness and constant hydrating solution on the ocular surface.

Drug formulations, devices and methods are provided to deliver biologically active substances to the eye. The formulations are delivered into scleral tissues adjacent to or into the suprachoroidal space without damage to the underlying choroid. One class of formulations is provided wherein the formulation is localized in the suprachoroidal space near the region into which it is administered. Another class of formulations is provided wherein the formulation can migrate to another region of the suprachoroidal space, thus allowing an injection in the anterior region of the eye in order to treat the posterior region.

Systems and methods are provided for generating and applying artificial tear film layers to a cornea surface. An example method includes forming an artificial tear film that is optically transparent, ultra-thin, and smoothly conforming to cornea surface. The artificial tear film includes a lipid layer that prevents evaporation of moisture from the cornea (e.g., from the underlying aqueous layer of the artificial tear film, and/or from the natural tear film on the cornea, etc.). A dispenser, such as an atomizer/nebulizer/micronizer, can be used to generate and applying the artificial tear film layers, especially the lipid layer, with reduced dispensing volume and average droplet size, etc., such that the deposit thickness of the artificial tear film layers remains thin and better spreads and conforms to the surface of the cornea, as compared to the results of conventional eye droppers dispensing conventional artificial tears.

An implant for insertion into a punctum of a patient comprises a body. The body has a distal end, a proximal end, and an axis therebetween. The distal end of the body is insertable distally through the punctum into the canalicular lumen. The body comprises a therapeutic agent included within an agent matrix drug core. Exposure of the agent matrix to the tear fluid effects an effective therapeutic agent release into the tear fluid over a sustained period. The body has a sheath disposed over the agent matrix to inhibit release of the agent away from the proximal end. The body also has an outer surface configured to engage luminal wall tissues so as to inhibit expulsion when disposed therein. In specific embodiments, the agent matrix comprises a non-bioabsorbable polymer, for example silicone in a non-homogenous mixture with the agent.

An ocular implant is provided. In some embodiments, the ocular implant includes a body that is curved about a longitudinal central axis and a distal body portion that defines a longitudinal channel including a channel opening. The implant is sized and configured such that the ocular implant assumes an orientation in which the channel opening is adjacent a major side of Schlemm’s canal when the ocular implant is disposed in Schlemm’s canal. Methods for delivering ocular implants into Schlemm’s canal are also provided. Some methods include covering openings in the ocular implant, advancing the implant into Schlemm’s canal while at least some of the openings are covered, and uncovering the openings while the distal portion of the implant is disposed in Schlemm’s canal.

According to one aspect of the disclosure, an apparatus for manipulating a sclera to facilitate delivery of a medicament to a suprachoroidal space of an eye may include a needle with a sharp distalmost tip, a needle hub connected to a proximal end of the needle, a housing surrounding the needle hub and extending from a proximal end of the needle hub, and an adaptor surrounding a portion of the needle.