IP Library Granted Patent US 9,387,099
Granted Patent B2
US 9,387,099 · App. 13/564,148 · Granted Jul 12, 2016

Non-woven helical wire stent

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Quick Facts
Patent No.
US 9,387,099
App. No.
13/564,148
Granted
Jul 12, 2016
Kind
B2
Abstract

Exemplary non-woven helical stents are described that are efficient to fabricate in terms of labor and resources by being able to be manufactured by hand or machine while providing mechanical stability equivalent or close thereto of known braided or woven stents.

Claims (29)

1. A stent comprising:

a first wire configured into a non-woven first longitudinal tube having a first helical pattern and comprising a proximal portion and a distal portion, and a lumen extending between the proximal portion and the distal portion, wherein the first longitudinal tube is outwardly biased to assume an expanded configuration; and

a second wire configured into a non-woven second longitudinal tube having a second helical pattern and comprising a proximal portion and a distal portion, and a lumen extending between the proximal portion and the distal portion, wherein the second longitudinal tube is inwardly biased to assume a compressed configuration;

wherein the first helical pattern of the first longitudinal tube is opposite to the second helical pattern of the second longitudinal tube;

wherein the second longitudinal tube is disposed about at least a portion of the first longitudinal tube in a non-woven manner; and

wherein the outwardly bias of the first longitudinal tube and the inwardly bias of the second longitudinal tube combine to form a mechanically stable assembled stent that is expandable from a compressed delivery configuration to an expanded deployed configuration.

2. The stent of claim 1 , further comprising a covering affixed to at least a portion of one of the first longitudinal tube or the second longitudinal tube.

3. The stent of claim 2 , wherein the covering comprises silicone.

4. The stent of claim 1 , further comprising a covering disposed between at least a portion of the first longitudinal tube and the second longitudinal tube.

5. The stent of claim 1 , wherein at least one of the first wire or the second wire comprises a shape-memory alloy.

6. The stent of claim 1 , wherein at least one of the first wire or the second wire comprises nitinol.

7. The stent of claim 1 , wherein the first wire of the first longitudinal tube comprises a first non-woven layer wound in a clockwise helical orientation; and wherein the second wire of the second longitudinal tube comprises a second non-woven layer wound in a counterclockwise helical orientation.

8. The stent of claim 1 , wherein the second wire of the second longitudinal tube comprises a second non-woven layer wound in a clockwise helical orientation; and wherein the first wire of the first longitudinal tube comprises a first non-woven wire wound in a counterclockwise helical orientation.

9. The stent of claim 1 , wherein the first wire comprises a first and second end and the second wire comprises a first and second end; wherein at least one of the first or second end of the first or second wire is secured by a weld.

10. The stent of claim 1 , wherein the first wire comprises a first and second end and the second wire comprises a first and second end; wherein at least one of the first or second end of the first or second wire is secured by a covering.

11. The stent of claim 1 , wherein the first wire comprises a first and second end and the second wire comprises a first and second end; wherein at least one of the first or second end of the first or second wire is secured by a securing means.

12. The stent of claim 1 , wherein the stent further comprises a proximal portion and a distal portion, wherein at least one of the proximal portion or the distal portion comprises a purse string attached thereto and configured to compress the stent.

13. The stent of claim 1 , wherein the stent further comprises a proximal portion and a distal portion, wherein at least one of the proximal portion or the distal portion is configured into a flared orientation.

14. The stent of claim 1 , wherein the first longitudinal tube comprises an overall length that is about equal to an overall length of the second longitudinal tube, and wherein the second longitudinal tube is disposed about the first longitudinal tube in a fully overlapping configuration.

15. The stent of claim 1 , wherein the first wire of the first longitudinal tube is separate from the second wire of the second longitudinal tube.

16. The stent of claim 1 , wherein the assembled stent is self-expandable from the compressed delivery configuration to the expanded deployed configuration.

17. The stent of claim 1 , wherein the assembled stent is mechanically expandable from the compressed delivery configuration to the expanded deployed configuration.

18. A non-woven stent comprising:

a first wire configured into a first non-woven longitudinal tube comprising a proximal portion and a distal portion, and a lumen extending between the proximal portion and the distal portion, wherein the first non-woven longitudinal tube is outwardly biased to assume an expanded configuration; and

a second wire configured into a second non-woven longitudinal tube comprising a proximal portion and a distal portion, and a lumen extending between the proximal portion and the distal portion, wherein the second non-woven longitudinal tube is inwardly biased to assume a compressed configuration;

wherein the first non-woven longitudinal tube and the second non-woven longitudinal tube each comprise a helical pattern, the helical pattern of the first non-woven longitudinal tube having a helical orientation opposite that of the helical pattern of the second non-woven longitudinal tube;

wherein the second non-woven longitudinal tube is disposed about at least a portion of the first non-woven longitudinal tube in a non-woven manner;

wherein the outwardly bias of the first non-woven longitudinal tube and the inwardly bias of the second non-woven longitudinal tube combine to form a mechanically stable assembled stent that is expandable from a compressed delivery configuration to an expanded deployed configuration; and

wherein the stent further comprises a proximal portion and a distal portion, wherein at least one of the proximal portion or the distal portion comprises a purse string attached thereto and configured to compress the stent.

Assignments (1)
SECURITY INTEREST Recorded Feb 28, 2024
From: COOK MEDICAL TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 066700/0277 →