Intended for healthcare professionals

SECURESTRAP™ Open Absorbable Strap Fixation Device

SECURESTRAP™ Open Absorbable Strap Fixation Device is the first absorbable fixation device purposefully designed for the unique challenge of open ventral hernia repair.1 It features a low profile design to reduce exposure to viscera.2 Each strap, from the first to the last, deploys with a similar force — providing the reliability you need.3

About this device

The SECURESTRAP™ Open Absorbable Strap Fixation Device is a trigger-squeeze mechanical device with a curved cannula, pre-loaded with 20 absorbable straps. The tip of the device is designed to facilitate the placement of prosthetic material using straps. The straps are made of a blend of polydioxanone and an L-lactide/glycolide copolymer, with an inserted length of 6.7mm.4

Specialties

Hernia

Procedures

Open intra-abdominal ventral hernia repair procedures

Features & benefits

Fixation at multiple angles

Fixation at multiple angles

Demonstrated greater acute holding strength at 30, 45, 60, and 90-degree angles compared to two different spiral constructs in absorbable fixation devices, based on bench top testing in porcine flank (p < 0.05).5

Efficient and less stress

Efficient and less stress

Deliver a more efficient and less stressful repair with an 89% reduction in fixation time and 55% reduction in surgical stress versus suture fixation alone.6

Reduced pain

Reduced pain

Proven to reduce patient pain post-hernia repair.7 Shown in a preliminary study of International Hernia Mesh Registry (IHMR) patients to provide an improvement in pain levels and movement limitations.7A

Learn how to use this device

SECURESTRAP™ Open Absorbable Strap Fixation Device

Supporting documentation

PDF

SECURESTRAP™ Absorbable Strap Fixation Device portfolio brochure

PDF

Hernia procedure brochure

PDF

Hernia value proposition
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Related products

PROCEED™ Surgical Mesh

PROCEED™ Surgical Mesh

Mesh optimized for strength and performance are critical for Intraperitoneal only mesh repair (IPOM) procedures. Trusted by surgeons for over a decade,A PROCEED™ Surgical Mesh is a macroporous, partially absorbable, tissue-separating mesh, combining large-pore mesh knitted with monofilament fibers and natural, absorbable tissue separating technology.1,2B

SECURESTRAP™ Absorbable Strap Fixation Device

SECURESTRAP™ Absorbable Strap Fixation Device

Tissue capture, penetration and holding strength at multiple deployment angles are important factors when selecting a fixation device for hernia repair.  SECURESTRAP™ Absorbable Strap Fixation Device is a market leading fixation device1A designed for acute holding strength at various deployment angles.2,3

ULTRAPRO ADVANCED™ Macroporous Partially Absorbable Mesh

ULTRAPRO ADVANCED™ Macroporous Partially Absorbable Mesh

Built on the proven technology of ULTRAPRO™ Macroporous Partially Absorbable Mesh1, ULTRAPRO ADVANCED™ is designed to help optimize patient outcomes2,3and ease of use4,5 in inguinal and ventral hernia repair. Physiologically designed for comfortable healing6-8, it features a unique knitted mesh construction to promote good tissue ingrowth/integration.9A

References

A. Prospective, longitudinal study of SECURESTRAP™ Fixation Device in hernia repair from the International Hernia Mesh Registry (IHMR). 88 patients (group 1) were treated with mechanical mesh fixation alone, and 98 patients with mechanical fixation + sutures (group 2). Hernia types (%) in group 1 and 2 were, respectively: incisional/ventral (43.2 and 74.5), umbilical (23.9 and 11.2), epigastric (11.4 and 4.1) and were mostly primary repairs (87.5 and 78.6) done laparoscopically (97.7 and 98.0). Most common adverse events, respectively: seroma (8.0% and 18.4%), hematoma (2.3% in group 1), procedural pain (2.3% and 2.0%), and urinary retention (2.0% in group 2). Hernia recurrences (up to 12 months) respectively: 1.1% (1 medically confirmed) and 7.1% (4 medically confirmed and 3 unconfirmed). Patients with symptomatic CCS pain and movement limitation scores, improved from baseline (70.9%; 61.1%) to 12 months (29.9%; 19.7%), respectively (p<0.001). A total of seventy-seven patients from groups 1 and 2 had 12-month data. The Carolinas Comfort Scale™ defines symptomatic pain as a greater than 1 (mild but not bothersome symptoms) for at least 1 question within the domains of severity of pain, sensation of mesh, or movement limitation.


  1. SECURESTRAP™ Open Absorbable Strap Fixation Device First Absorbable Fixation Device for Open Ventral Design Memo, September 17, 2025.
  2. Ethicon, ORN-50-3090 Tack Comparison CAD Surface Area Drawing, April 2010.
  3. SECURESTRAP™ Design Reliability Memo, May 3, 2010. DOCUMENT: 25/2-65674 TRIM database.
  4. SECURESTRAP™ Open Absorbable Strap Fixation Device Instructions for Use. Ethicon, Inc.
  5. Ethicon, SEC-339-11-8-13 Comparison of Acute Holding Strength of an Absorbable Strap. 30 August, 2011.
  6. Roy S, Shnoda P, Savidge S, Hammond J, Panish J, Wilson M. Reduction in fixation time and related surgical stress with the use of ETHICON SECURESTRAP™ Open Absorbable Strap Fixation Device in the deployment of intra-peritoneal onlay mesh (IPOM) for open ventral hernia repair. Paper presented at: ISPOR 16th Annual European Congress; November 2-6, 2013; Dublin, Ireland.
  7. Doerhoff C, Chudy M, Gauld J, et al. Preliminary Outcomes using an absorbable fixation device for mesh fixation. AHS 2013 SECURESTRAP (poster).

Clinical and technical support is available 24/7 at 1-877-ETHICON (384-4266)

The third-party trademarks used herein are trademarks of their respective owners. 

For complete indications, contraindications, warnings, precautions, and adverse reactions, please reference full package insert. 


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