IP Library Granted Patent US 7,353,683
Granted Patent B2
US 7,353,683 · App. 11/048,354 · Granted Apr 8, 2008

Surgical needle manufacturing process

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Quick Facts
Patent No.
US 7,353,683
App. No.
11/048,354
Granted
Apr 8, 2008
Kind
B2
Abstract

A process for manufacturing a surgical needle incorporates at least one pressing operation which, preferably, in conjunction with a trimming and/or etching process, ultimately forms the sharpened needle end. The grinding operation in the preferred process does not produce the primary sharpened edges of the needle, but, rather is incorporated, in one instance, to reduce excess needle material prior to the pressing operation. Consequently, the amount of flash material generated during pressing is substantially reduced. This feature desirably enhances the subsequent trimming and etching operations, and produces a needle which is extremely sharp, durable and exhibits an improved retention of sharpness over periods of prolonged use.

Claims (38)

1. A process for manufacturing a surgical needle, comprising the steps of:

providing a surgical needle blank, the needle blank comprising a biocompatible material;

coining the needle blank to define a needle end having first, second and third sides;

removing needle material from the needle end;

providing a die mechanism having a die arrangement with a die concavity therein and a die punch positioned in opposition to the die concavity, the die punch having a radiused surface;

positioning the needle end within the die concavity with the first side of the needle end in opposed relation to the die punch;

pressing the needle end by activating the die mechanism whereby the radiused surface of the die punch imparts an arcuate surface on the first side of the needle end; and

forming cutting edges adjacent areas of intersection between the first, second and third sides to define a plurality of cutting edges on the needle end.

2. The process according to claim 1 wherein the step of removing the needle material includes grinding at least the second side of the needle end to remove material adjacent the second side of the needle end.

3. The process according to claim 2 wherein the step of removing the needle material includes grinding the third side of the needle end to remove material adjacent the third side of the needle end.

4. The process according to claim 1 , the die concavity defines a tapered characteristic whereby the cross-sectional area occupied by the concavity decreases from one end of the concavity to the other end of the concavity and wherein the step of pressing imparts a tapered configuration to the needle end.

5. The process according to claim 4 wherein the die concavity of the die mechanism defines a general triangular configuration having first and second pressing surfaces and wherein the step of pressing includes positioning the needle blank within the concavity of the die mechanism to impart a generally tapered triangular-shaped cross-section to the needle end.

6. The process according to claim 1 wherein during the step of pressing, excess needle flash material is created adjacent the areas of intersection of the first and second sides, and the first and third sides of the needle end.

7. The process according to claim 6 including the step of trimming the flash material from the areas of intersection.

8. The process according to claim 7 wherein the step of trimming includes forming a crease line along each of the areas of intersection of the first and second sides, and the first and third sides of the needle end, the crease lines adapted to provide at least two cutting edges.

9. The process according to claim 8 including the step of etching the needle end to further remove flash material and sharpen the cutting edges.

10. The process according to claim 9 wherein the step of etching includes introducing a first current into the acid bath for a first determining period of time and introducing a second current into the acid bath for a second predetermined period of time.

11. The process according to claim 8 including the step of flat pressing the needle blank subsequent to the step of pressing the needle end.

12. The process according to claim 11 wherein the flat press includes at least one die, the at least one die defining a die cavity having a pressing surface, the pressing surface inclined relative to an axis of the at least one die whereby, during the step of pressing, the pressing surface impacts the needle end to cause needle material to flow such that at least portions of the at least two cutting edges extend beyond a perimeter of the body of the needle blank.

13. The process according to claim 8 including the step of heat treating the needle blank.

14. The process according to claim 5 wherein the first and second pressing surfaces of the die concavity are substantially planar and wherein the step of pressing includes imparting planar surfaces on the second and third sides of the needle end.

15. The process according to claim 8 wherein the step of trimming includes providing a trim die mechanism defining a die recess and having opposed raised protrusions adjacent the die recess and including the step of positioning the needle end within the die recess and pressing the needle end whereby the raised protrusions form the crease lines along respective areas of intersection.

16. A process for manufacturing a surgical needle, comprising the steps of:

providing a surgical needle blank, the needle blank comprising a biocompatible material;

coining the needle blank to define a coined needle end having first, second and third sides;

removing needle material from the coined needle end;

positioning the coined needle end within a die arrangement of a die mechanism and

pressing the first side of the coined needle end with a die punch of the die mechanism, the die punch having a radiused surface to impart an arcuate surface on the first side of the needle end and to produce intersecting surface portions between the first, second and third sides of the coined needle end; and

forming cutting edges adjacent areas of intersection of the surface portions.

17. The process according to claim 16 wherein the step of removing includes grinding the coined needle end.

18. A process for manufacturing a surgical needle comprising the steps of:

providing a needle blank;

coining the needle blank to define a needle end having first, second and third sides;

pressing the first, second and third sides of the needle end within a press die mechanism to impart a generally tapered triangular cross-section to the needle end;

positioning the needle end within a trim die mechanism having a trim die cavity and opposed raised protrusions adjacent each side of the trim die cavity;

activating the trim die mechanism to impart crease lines within needle overflow material adjacent an area of between the first and the second sides of the needle end and adjacent an area between the first and third sides of the needle end; and

forming cutting edges along the crease lines of the needle end.

19. The process according to claim 18 wherein the step of forming cutting edges includes etching the needle end to facilitate removal of the needle overflow material adjacent the crease lines.

Assignments (3)
CHANGE OF NAME Recorded Oct 2, 2012
From: TYCO HEALTHCARE GROUP LP
To: COVIDIEN LP
Reel/Frame 029065/0448 →
CORRECTIVE COVERSHEET TO CORRECT SERIAL NUMBER 10/764,103 PREVIOUSLY RECORDED AT REEL 016390, FRAME 0557 OF ASSIGNOR MICHAEL W. BOGART Recorded Sep 1, 2005
From: BOGART, MICHAEL W.
To: TYCO HEALTHCARE GROUP, LP
Reel/Frame 016948/0917 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2005
From: BOGART, MICHAEL W.
To: TYCO HEALTHCARE GROUP LP
Reel/Frame 016390/0557 →