Nasal dilation respiratory device and system

A nasal dilation respiratory device configured to be attached to a user's nose to dilate a nasal cavity, comprising:

• a support member configured to be provided adjacent to a nasal region of the user, the support member comprising two end portions, an intermediate portion, and at least one attachment surface;
• wherein the two end portions are respectively formed at opposite ends of the support member;
• wherein the intermediate portion is provided between the two end portions and is configured to correspond to a region between a nasal bridge and a nasal tip of the user during use;
• and
• wherein the at least one attachment surface is provided on a surface of at least one of the two end portions and is configured to connect with at least one connecting member;
• and
• at least one connecting member comprising a first portion and a second portion, wherein the first portion is configured to be at least partially attached to at least one lateral region of the user's nose, and wherein the second portion of the connecting member is configured to be detachably adhered to the at least one attachment surface of the support member via hook-and-loop fastening.

A nasal dilation respiratory device configured to be attached to a user's nose to dilate a nasal cavity, comprising:

• a support member configured to be provided adjacent to a nasal region of the user, the support member comprising two end portions, an intermediate portion, and at least one attachment surface;
• wherein the two end portions are respectively formed at opposite ends of the support member;
• wherein the intermediate portion is provided between the two end portions and is configured to correspond to a region between a nasal bridge and a nasal tip of the user during use;
• and
• wherein the at least one attachment surface is at least partially attached to at least one of the two end portions by mechanical connection, chemical bonding, and/or integrally molding;
• and
• at least one connecting member comprising a first portion and a second portion, wherein the first portion is configured to be at least partially attached to at least one lateral region of the user's nose, and wherein the second portion is configured to be connected to the at least one attachment surface so as to detachably connect the support member to the at least one connecting member via hook-and-loop fastening, clasps, magnetic attraction, or chemical adhesive bonding;
• wherein the respiratory device comprises at least one of the following characteristics:
• the support member has a thickness of at least a portion thereof within a range of 0.1 mm to 20 mm;
• the support member has a length within a range of 9 mm to 150 mm;
• the support member has an angle within a range of 30 degrees to 180 degrees;
• and
• an area of the at least one connecting member attached to the user's nose is within a range of 0.05 cm2 to 20 cm2.

A nasal dilation respiratory system configured to assist a user in dilating a nasal cavity, comprising:

• a support member configured to be provided adjacent to a nasal region of the user, the support member comprising:
• two end portions respectively formed at opposite ends of the support member and configured to correspond to outer regions of the user's nasal alae during use;
• and
• an intermediate portion provided between the two end portions and configured to correspond to a region between a nasal bridge and a nasal tip of the user during use;
• at least one attachment surface on a surface of at least one of the two end portions and configured to connect with at least one connecting member;
• and
• the at least one connecting member, comprising:
• a first portion configured to be at least partially attached to at least one lateral region of the user's nose;
• and
• a second portion of the connecting member configured to be detachably adhered to the at least one attachment surface via hook-and-loop fastening;
• wherein a connection force generated between the support member and the at least one connecting member ranges from 2 gf to 200 gf;
• and
• wherein a nasal cavity dilation amplitude generated during use ranges from 0.1 mm to 20 mm.