Each is on the Department of Defense Committee on Tactical Combat Casualty Care (CoTCCC) list of recommended devices, and each is a medical device regulated by the U.S. Food and Drug Administration. They are listed below in no particular order.

SAM XT Extremity Tourniquet on a plain background. Named device only. No injury imagery.

SAM® XT Extremity Tourniquet

SAM Medical · Windlass with auto-locking buckle

A buckle that locks automatically once the strap reaches a set tension, so the band is seated tightly before the windlass is turned.

  • Program-accepted
  • CoTCCC-recommended
  • FDA-regulated medical device
  • Tension-set buckle
Tactical Mechanical Tourniquet (TMT) on a plain background. Named device only. No injury imagery.

Tactical Mechanical Tourniquet (TMT®)

Alphapointe · Windlass with metal buckle

A 2" wide band held open by a stiffened strap so it does not collapse while being positioned, with a separating buckle for lower limb application and integrated windlass lock. It can be applied one-handed if needed.

  • Program-accepted
  • CoTCCC-recommended
  • FDA-regulated medical device
  • Hinged locking bar
SOF Tactical Tourniquet Wide (SOFTT-W) on a plain background. Named device only. No injury imagery.

SOF® Tactical Tourniquet Wide (SOFTT-W)

TacMed Solutions · Windlass with hinged locking bar

A wide, reinforced band with an aluminum windlass and an opening buckle that allows the tourniquet to be placed directly around a limb without sliding it over the hand or foot. Designed for rapid one- or two-handed application.

  • Program-accepted
  • CoTCCC-recommended
  • FDA-regulated medical device
  • Buckle opens for routing
Combat Application Tourniquet (C-A-T) on a plain background. Named device only. No injury imagery.

Combat Application Tourniquet® (C-A-T®)

North American Rescue · Windlass with locking clip

A self-adhering band tightened by a rod, which is then locked into a plastic clip. It can be applied one-handed to the user’s own arm.

  • Program-accepted
  • CoTCCC-recommended
  • FDA-regulated medical device
  • One-handed capable

Medical devices, not accessories

What “accepted” means for a tourniquet

A tourniquet is a medical device. Each of the four above is manufactured by a company registered with the U.S. Food and Drug Administration and is listed with the FDA as a medical device under 21 CFR Part 807. Each also appears on the CoTCCC recommended devices list, which is the Department of Defense’s evidence-based reference for battlefield trauma care. The program accepts tourniquets from that list that a member of the public can apply with the training the STOP THE BLEED® class provides.

Only these four may be packed in a STOP THE BLEED® kit. A licensee cannot substitute another tourniquet, and a tourniquet sold on its own under the STOP THE BLEED® name must be one of the four. Counterfeit copies of these devices are common in online marketplaces and can fail under load; buy from a licensed seller, and if the price or packaging seems off, look more closely.

These notes are only here to help you tell the four apart. They are not instructions, and none of the four is recommended over the others. Put a tourniquet on the way your STOP THE BLEED® class taught you and the way the directions on the package say. Find a class near you.