Embolic beads

Occlusin 500

by IMBiotechnologies Ltd

A bioabsorbable, implantable bead/microsphere intended to be used to temporarily occlude an artery supplying hyperplastic/neoplastic tissue in a variety of anatomies (e.g., liver, lung, breast, bladder, uterus, head or neck); it does not include a pharmaceutical agent. It may be used independently to create ischemia in the tissue, or as an adjuvant in combination with cytostatic agents and other antitumour drugs to help optimize intra-tumour drug accumulation for interventional radiology and visceral surgery procedures. It is typically available as an injectable solution containing numerous microspheres [e.g., degradable starch microspheres (DSM)].

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Occlusin 500 models and sizes

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

Model / catalog no.SizeMRIStatus
Ekobi 501β€” Not statedAvailable
Ekobi 502β€” Not statedAvailable
Ekobi 503β€” Not statedAvailable
Ekobi 503Lβ€” Not statedAvailable
Ekobi 503Pβ€” Not statedAvailable
Ekobi 504β€” Not statedAvailable
Ekobi 505β€” Not statedAvailable

FDA clearances

  • 510(k) K093813 May 2010

Procedures that use embolic beads

Frequently asked questions

What is Occlusin 500 used for?

A bioabsorbable, implantable bead/microsphere intended to be used to temporarily occlude an artery supplying hyperplastic/neoplastic tissue in a variety of anatomies (e.g., liver, lung, breast, bladder, uterus, head or neck); it does not include a pharmaceutical agent. It may be used independently to create ischemia in the tissue, or as an adjuvant in combination with cytostatic agents and other antitumour drugs to help optimize intra-tumour drug accumulation for interventional radiology and visceral surgery procedures. It is typically available as an injectable solution containing numerous microspheres [e.g., degradable starch microspheres (DSM)].

Who makes Occlusin 500?

Occlusin 500 is made by IMBiotechnologies Ltd. It is listed under embolic microspheres and particles (beads) in our device library.

What sizes does Occlusin 500 come in?

The FDA device database does not list sizes for Occlusin 500. Check the instructions for use or ask a IMBiotechnologies Ltd representative.

Is Occlusin 500 MRI safe?

The FDA device database entry for Occlusin 500 does not state its MRI safety status. Check the labeling before MRI.

Is Occlusin 500 FDA cleared?

Occlusin 500 is covered by FDA submission K093813.

How do I contact a IMBiotechnologies Ltd sales representative?

IMBiotechnologies Ltd has not listed representatives on LA Vascular yet. Visit the IMBiotechnologies Ltd 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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