IP Library Granted Patent US 8,556,926
Granted Patent B2
US 8,556,926 · App. 13/297,719 · Granted Oct 15, 2013

Total occlusion guidewire device

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Quick Facts
Patent No.
US 8,556,926
App. No.
13/297,719
Granted
Oct 15, 2013
Kind
B2
Abstract

A guidewire having a spreader or at least one centering device which may be used to open occluded vessels or other biological passages, especially chronic total occlusions. The guidewire may be used to either open the lumen or to center a boring device within the lumen, so that the chronic total occlusion can be crossed, and an interventional procedure can then be performed.

Claims (18)

1. A guidewire for insertion into a lumen, said guidewire comprising:

a flexible wire having an outer diameter, an inner diameter, a proximal end and a distal end;

a generally solid, rotatable core wire having an outer diameter, a proximal end and a distal end, with said distal end of said rotatable core wire slidably inserted into said proximal end of said flexible wire;

a guide tip attached to said distal end of said rotatable core wire, wherein said guide tip comprises a boring surface; and

a sheath, having an outer diameter and an inner diameter, a proximal end and a distal end, with said distal end of said sheath slidably insertable over said proximal end of said flexible wire,

at least one centering device attached to said distal end of said flexible wire, said at least one centering device having a proximal end and a distal end, a smaller first diameter for insertion into said lumen, and a second larger diameter for centering said flexible wire in said lumen, said at least one centering device having said smaller first diameter when said sheath is slidably inserted over said flexible wire and said centering device, until said distal end of said sheath is substantially in contact with said guide tip, and said at least one centering device having said second larger diameter when said sheath is slidably retracted from said guide tip until said distal end of said sheath is no longer in contact with said at least one centering device.

2. The guidewire according to claim 1 , wherein there are a plurality of centering devices.

3. The guidewire according to claim 2 , wherein each of said plurality of centering devices has a proximal end and a distal end, a smaller first diameter for insertion into said lumen, and a second larger diameter for centering said flexible wire in said lumen.

4. The guidewire according to claim 1 , wherein said flexible wire is made from super-elastic Nickel-Titanium alloy.

5. The guidewire according to claim 1 , wherein said flexible wire incorporates segments made from a polymeric material.

6. The guidewire according to claim 1 , wherein said at least one centering device is made from super-elastic Nickel Titanium alloy.

7. The guidewire according to claim 1 , wherein said flexible wire and said at least one centering device are both made from super-elastic Nickel-Titanium alloy.

8. The guidewire according to claim 1 , wherein said at least one centering device comprises a proximal portion and a distal portion, and a plurality of longitudinal struts extending therebetween.

9. The guidewire according to claim 1 , wherein said at least one centering device comprises a proximal portion and a distal portion, and a plurality of circumferential struts extending in a spiral pattern therebetween.

10. The guidewire according to claim 1 , wherein said at least one centering device comprises a proximal portion and a distal portion, and a plurality of hingedly connected struts extending therebetween.

11. The guidewire according to claim 1 , wherein said sheath is made from a polymeric material.

12. The guidewire according to claim 1 , wherein said at least one centering device is permanently or removably attached to said distal end of said flexible wire.

13. The guidewire according to claim 1 , wherein said boring guide tip is permanently or removably attached to said distal end of said rotatable core wire.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2025
From: CARDINAL HEALTH SWITZERLAND 515 GMBH; CARDINAL HEALTH 529, LLC; CORDIS CORPORATION; FLEXIBLE STENTING SOLUTIONS, INC
To: CORDIS US CORP
Reel/Frame 072987/0675 →