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Ranfac RSG-14 — single-use puncture closure device for laparoscopic trocar site closure
FDA Cleared · K032478 Single Use · Sterile EO Latex-Free
General Surgery · Trocar Site Closure

RSG-14 Puncture Closure Device

The RSG-14 is a single-use percutaneous puncture-closure device for laparoscopic trocar site management. Designed to deliver and capture suture through the abdominal fascia for secure closure of port sites.

CatalogRSG-14
Part #76004-01M
DevicePuncture Closure
UseSingle Use
SterilitySterile (EO)
ClearanceK032478

Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.

Overview

The Ranfac RSG-14 is a single-use percutaneous puncture-closure device for laparoscopic trocar site management. The instrument carries suture through the abdominal fascia and recaptures it on the opposite side, allowing the surgeon to close port sites under direct visualization. Each device ships sterile, ethylene-oxide processed, and individually packaged.

The RSG-14 is part of the Ranfac surgical-instrument portfolio for laparoscopic and percutaneous procedures. It pairs with the rest of the Ranfac MIS family — insufflation (IN-12), percutaneous introducer (PIN-15), and cholangiography catheters (LAP-13, XL-11) — across the standard laparoscopic workflow.

Clinical Applications

Refer to the device Instructions for Use (IFU, 76004-01M Rev C) for the full indications, contraindications, warnings, and step-by-step procedure. The device is intended for the surgical closure of laparoscopic trocar puncture sites.

Surgeons use puncture-closure devices for secure fascia closure at laparoscopic trocar sites, particularly at port sites ≥10 mm where fascial closure reduces the risk of postoperative hernia. The RSG-14 supports closure under direct laparoscopic visualization.

Laparoscopic Surgery

Trocar site fascia closure at ≥10 mm ports during general laparoscopic procedures.

Bariatric & Foregut

Port-site closure where postoperative hernia risk is elevated due to BMI or port size.

Gynecology & Urology

Pelvic laparoscopic port-site management.

Standard MIS Workflows

Used across general, bariatric, gynecologic, and urologic laparoscopic procedures where the device is part of the surgeon's standard instrument set.

Specifications

RSG-14 Technical Data

Construction, regulatory, and packaging details. Gauge, length, cannula and stylet are listed in the hero above. For complete indications, contraindications, and warnings, download the Instructions for Use.

ConstructionStainless steel components · medical-grade polymer hub
ConnectionStandard luer connections per device IFU
SterilizationEthylene oxide · single-use · latex-free
PackagingIndividually pouched
FDA Clearance510(k) K032478 · Class II
PrescriptionRx only (21 CFR 801 Subpart D)

Directions for Use (Summary)

The following is a high-level summary. Refer to the IFU (76004-01M Rev C) for complete instructions, contraindications, and warnings.

  1. Inspect packaging. Confirm integrity; if undamaged, open using aseptic technique.
  2. Inspect the device. Verify mechanism function and component integrity prior to use.
  3. Load suture into the device per the IFU diagram.
  4. Position the device at the trocar site to be closed.
  5. Advance through fascia under laparoscopic visualization on one side of the defect.
  6. Release suture into the peritoneal cavity per IFU procedure.
  7. Withdraw and reposition on the opposite side of the fascial defect.
  8. Recapture suture and withdraw through the abdominal wall.
  9. Tie and dispose. Complete the fascial closure and dispose of the used device in a sharps biohazard container per facility policy.

Documents & Downloads

Frequently Asked Questions

What is the RSG-14 used for?

Closure of laparoscopic trocar puncture sites — specifically fascia closure at port sites ≥10 mm to reduce postoperative hernia risk.

Is the RSG-14 FDA cleared?

Yes, under 510(k) K032478 as a Class II surgical instrument. Refer to the device IFU and 510(k) clearance letter for full regulatory status.

Is the device reusable?

No. The RSG-14 is a single-use device — supplied sterile and disposed of after a single procedure per facility policy.

What sterilization method is used?

Ethylene oxide (EO). The device is shipped sterile and is not made with natural rubber latex.

Is the RSG-14 compatible with any suture size?

The RSG-14 is designed to deliver and recapture standard surgical suture per the device IFU. For specific suture-size compatibility, refer to the Instructions for Use (76004-01M Rev C) in the Documents section below.

Where can I find detailed instructions?

The Instructions for Use (IFU, document 76004-01M Rev C) is available in the Documents & Downloads section below.

Related Products

Other configurations in the Ranfac General Surgery family.

IN-12 — IN-12 Insufflation Needle (12 cm)

IN-12

Single-use 12 cm insufflation needle for laparoscopic pneumoperitoneum establishment

View →
PIN-15 — PIN-15 Percutaneous Introducer Needle

PIN-15

Single-use percutaneous introducer needle for guidewire placement and percutaneous access

View →
LAP-13 — LAP-13 Cholangiography Catheter (Port Access)

LAP-13

Single-use cholangiography catheter for laparoscopic intraoperative bile duct imaging via trocar port access

View →
XL-11 — XL-11 Cholangiography Catheter (Percutaneous Access)

XL-11

Single-use cholangiography catheter for percutaneous intraoperative bile duct imaging

View →

Order or Request a Sample of the RSG-14

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Building a different device on the same platform? Ranfac runs custom OEM, CDMO, and CMO programs from concept through commercial. Talk to us about a custom configuration →