Comparison

Four categories of hemostatic dressing

Hemostatic gauze is not one category. The four families on the market differ in what they are made from, how many mechanisms they act through, and what they demand from the clinician applying them.

The landscape

The four product categories

WoundClot®

NONRCS

Non-oxidized, non-regenerated cellulose. No active ingredient — the substrate itself is hemostatic. Four mechanisms of action. FDA cleared, Rx Only.

Alternative 01

Oxidized regenerated cellulose

Cellulose broken down by oxidization. 75+ year-old technology. Representative products: Surgicel® and its variants.

Alternative 02

Kaolin / mineral

Non-resorbable non-woven fiber impregnated with kaolin, an inorganic clay. Representative product: QuikClot®.

Alternative 03

Chitosan

Non-resorbable non-woven fiber impregnated with chitosan, a sugar derived from crustacean exoskeleton. Representative products: Celox®, ChitoGauze®.

Side by side

Category comparison

Comparative statements below describe the product categories as characterized by the manufacturer of WoundClot®. Always confirm against the current Instructions for Use for any specific device.

Absorptive capacity, as a proportion of dressing weight

Bar lengths are drawn to the true ratio.

WoundClot® NONRCSNon-oxidized, non-regenerated cellulose

2,500%

Conventional hemostatic gauzeKaolin, chitosan and ORC carriers

~400%
The 2,500% figure is published by the manufacturer. The comparative figure is a manufacturer estimate for the product category as a whole, not a measured value for any single named device, and is presented here on that basis.
WoundClot® NONRCS compared with the three established hemostatic dressing categories.
Attribute WoundClot® — NONRCS Oxidized regenerated cellulose Kaolin / mineral Chitosan
Base material Cellulose broken down by oxidization Synthetic non-woven fiber + inorganic clay Synthetic non-woven fiber + shellfish-derived sugar
Active ingredient None — relies on oxidized substrate Kaolin Chitosan
Mechanisms of action Substrate-dependent; low absorptive contribution One — activation of Factor XII One — electrostatic attraction of red blood cells
Adjunctive pressure required Manual pressure typically applied Intense pressure, 3–5 min Sustained pressure required
Absorptive capacity Substantially reduced by oxidization Carrier-dependent; not the primary mechanism Carrier-dependent; not the primary mechanism
Duration of activity Not indicated for persistent or heavy bleeding Single-event activation Single-event activation
Re-bleeding on removal Adheres to gloves and instruments rather than wound surfaces May cause re-bleeding Product-dependent
Anticoagulated / coagulopathic patients Limited — designed for capillary and small-vessel oozing Dependent on an intact clotting cascade Dependent on red blood cell interaction
Residue & particulate Resorbable, but IFU advises removal where possible Kaolin may leach into the bleeding site Shellfish-derived — relevant to allergy screening
Thermal reaction None None in current-generation gauze formats None
Bleeding severity indicated Not designed for persistent or heavy bleeding Moderate to severe Moderate to severe

Surgicel® is a registered trademark of Ethicon, Inc. QuikClot® is a registered trademark of Z-Medica, LLC. Celox® is a registered trademark of Medtrade Products Ltd. ChitoGauze® is a registered trademark of Tricol Biomedical, Inc. These marks are used for identification only; Hemovance and Core Scientific Creations Ltd. are not affiliated with, endorsed by or sponsored by these companies.

In detail

What separates each category

vs. oxidized regenerated cellulose

ORC hemostats rest on technology more than seventy-five years old. They tend to adhere to gloved hands and instruments rather than to the intended wound surface, and they are not designed for use where persistent or heavy bleeding is occurring. Some ORC products are FDA Class III surgical implantables, yet their Instructions for Use direct removal wherever possible because of the raised risk of infection or adverse reaction.

WoundClot® leaves the cellulose structure unoxidized, which preserves absorbency (up to 2,500% of its weight) and adhesion to wound surfaces even under high-pressure bleeding.

vs. kaolin / mineral

Kaolin is an inorganic white clay produced by the natural decomposition of other clays or feldspar, carried on a non-resorbable non-woven fiber. These products work through a single mechanism — activation of Factor XII — and require intense manual pressure for at least three to five minutes to be effective.

WoundClot® requires only hand weight or placement pressure, adds three further mechanisms, and does not leach mineral into the bleeding site.

vs. chitosan

Chitosan is a sugar obtained from the hard outer skeleton of shellfish — crab, lobster and shrimp. Chitosan dressings work through a single mechanism: a positively charged agent attracting negatively charged red blood cells. Effectiveness therefore tracks with the patient's red cell interaction.

WoundClot® contains no shellfish-derived material, and its multiple mechanisms mean hemostasis does not rest on a single interaction.

Value analysis

Consolidation across departments

Because a single dressing is indicated across mild, moderate and severe bleeding — and works on anticoagulated and coagulopathic patients — it can consolidate products that are currently stocked separately by the operating room, the emergency department, dialysis, interventional radiology and the wound care team.

The manufacturer positions WoundClot® at approximately half the unit cost of Surgicel® and QuikClot®. Actual delivered cost depends on configuration, contract and volume — request a quote and we will model it against your current spend.

Documentation available for value analysis committees

  • Biocompatibility results summary (US)
  • ORC comparison chart
  • Peer-reviewed publications and case reports
  • Specialty primers — trauma, orthopedic, plastic, podiatry, ED, chronic wound
  • In-service education for clinical staff