G-tubes
EndoVive One Step Button
by Boston Scientific Corporation
A collection of devices which includes a gastrostomy tube with a pharmaceutical agent intended for short- and/or long-term (= 24 hours) access to the stomach via a gastrostomy. In addition to the gastrostomy tube and a pharmaceutical agent, the kit includes additional invasive devices designed to perform the gastrostomy and/or assist tube introduction (e.g., scalpel, introduction needle, stoma sizer, guidewire, dilator). This is a single-use device.
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Where to buy EndoVive One Step Button
Contact Boston Scientific Corporation directly; they can quote, ship, or point you to the distributor for your country.
From bostonscientific.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
EndoVive One Step Button models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| M00509580 | — | Not stated | Available |
| M00509590 | — | Not stated | Available |
| M00509600 | — | Not stated | Available |
| M00509610 | — | Not stated | Available |
| M00509620 | — | Not stated | Available |
| M00509630 | — | Not stated | Available |
| M00509680 | — | Not stated | Available |
| M00509690 | — | Not stated | Available |
| M00509700 | — | Not stated | Available |
| M00509710 | — | Not stated | Available |
| M00509720 | — | Not stated | Available |
| M00509730 | — | Not stated | Available |
| M00509740 | — | Not stated | Available |
| M00509750 | — | Not stated | Available |
| M00563010 | — | Not stated | Available |
| M00563020 | — | Not stated | Available |
| M00563030 | — | Not stated | Available |
| M00563040 | — | Not stated | Available |
| M00563080 | — | Not stated | Available |
| M00563090 | — | Not stated | Available |
| M00563100 | — | Not stated | Available |
| M00563120 | — | Not stated | Available |
| M00563130 | — | Not stated | Available |
| M00563140 | — | Not stated | Available |
| M00563150 | — | Not stated | Available |
| M00563160 | — | Not stated | Available |
| M00563180 | — | Not stated | Available |
| M00563190 | — | Not stated | Available |
| M00568450 | — | Not stated | Available |
| M00568460 | — | Not stated | Available |
| M00568470 | — | Not stated | Available |
| M00568480 | — | Not stated | Available |
| M00568500 | — | Not stated | Available |
| M00568510 | — | Not stated | Available |
| M00568520 | — | Not stated | Available |
| M00568530 | — | Not stated | Available |
Procedures that use g-tubes
Frequently asked questions
What is EndoVive One Step Button used for?
A collection of devices which includes a gastrostomy tube with a pharmaceutical agent intended for short- and/or long-term (= 24 hours) access to the stomach via a gastrostomy. In addition to the gastrostomy tube and a pharmaceutical agent, the kit includes additional invasive devices designed to perform the gastrostomy and/or assist tube introduction (e.g., scalpel, introduction needle, stoma sizer, guidewire, dilator). This is a single-use device.
Who makes EndoVive One Step Button?
EndoVive One Step Button is made by Boston Scientific Corporation. It is listed under gastrostomy and gj tubes in our device library.
What sizes does EndoVive One Step Button come in?
The FDA device database does not list sizes for EndoVive One Step Button. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is EndoVive One Step Button MRI safe?
The FDA device database entry for EndoVive One Step Button does not state its MRI safety status. Check the labeling before MRI.
Is EndoVive One Step Button FDA cleared?
EndoVive One Step Button 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.