Angioplasty balloons

Sterling SL

by Boston Scientific Corporation

A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.

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Where to buy Sterling SL

Contact Boston Scientific Corporation directly; they can quote, ship, or point you to the distributor for your country.

From bostonscientific.com, checked October 2026.

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Sterling SL models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
H74939147201010β€” Not statedAvailable
H74939147201090β€” Not statedAvailable
H74939147201210β€” Not statedAvailable
H74939147201290β€” Not statedAvailable
H74939147201510β€” Not statedAvailable
H74939147201590β€” Not statedAvailable
H74939147208010β€” Not statedAvailable
H74939147208090β€” Not statedAvailable
H74939147251010β€” Not statedAvailable
H74939147251090β€” Not statedAvailable
H74939147251210β€” Not statedAvailable
H74939147251290β€” Not statedAvailable
H74939147251510β€” Not statedAvailable
H74939147251590β€” Not statedAvailable
H74939147258010β€” Not statedAvailable
H74939147258090β€” Not statedAvailable
H74939147301010β€” Not statedAvailable
H74939147301090β€” Not statedAvailable
H74939147301210β€” Not statedAvailable
H74939147301290β€” Not statedAvailable
H74939147301510β€” Not statedAvailable
H74939147301590β€” Not statedAvailable
H74939147308010β€” Not statedAvailable
H74939147308090β€” Not statedAvailable
H74939147351010β€” Not statedAvailable
H74939147351090β€” Not statedAvailable
H74939147351210β€” Not statedAvailable
H74939147351290β€” Not statedAvailable
H74939147351510β€” Not statedAvailable
H74939147351590β€” Not statedAvailable
H74939147358010β€” Not statedAvailable
H74939147358090β€” Not statedAvailable
H74939147401010β€” Not statedAvailable
H74939147401090β€” Not statedAvailable
H74939147401210β€” Not statedAvailable
H74939147401290β€” Not statedAvailable
H74939147401510β€” Not statedAvailable
H74939147401590β€” Not statedAvailable
H74939147408010β€” Not statedAvailable
H74939147408090β€” Not statedAvailable

Procedures that use angioplasty balloons

Frequently asked questions

What is Sterling SL used for?

A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.

Who makes Sterling SL?

Sterling SL is made by Boston Scientific Corporation. It is listed under peripheral angioplasty balloons in our device library.

What sizes does Sterling SL come in?

The FDA device database does not list sizes for Sterling SL. Check the instructions for use or ask a Boston Scientific Corporation representative.

Is Sterling SL MRI safe?

The FDA device database entry for Sterling SL does not state its MRI safety status. Check the labeling before MRI.

Is Sterling SL FDA cleared?

Sterling SL is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Boston Scientific Corporation sales representative?

Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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