Endomina EZFuse system
Summary
Endo Tools Therapeutics S.A. received 510(k) clearance for Endomina EZFuse system, a OCW device. Cleared on 2026-02-13.
Details
Source
510(k) Clearance
External ID
K252400
Action Date
2026-02-13
Status
Traditional
Category
device
Product Code
OCW
Product Description
Endomina EZFuse system. Product code: OCW.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Endo Tools Therapeutics S.A. has received 2 total clearances in our database.
Endo Tools Therapeutics S.A. has 2 FDA actions in our database, including 2 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Endo Tools Therapeutics S.A. have FDA actions?
Endo Tools Therapeutics S.A. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252400" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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