RecallHawk

Artelon Convenience Kits

International Life Sciences

Summary

International Life Sciences received 510(k) clearance for Artelon Convenience Kits, a QWJ device. Cleared on 2026-04-09.

Details

Source

510(k) Clearance

External ID

K260317

Action Date

2026-04-09

Status

Traditional

Category

device

Product Code

QWJ

Product Description

Artelon Convenience Kits. Product code: QWJ.

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.

International Life Sciences has 4 FDA actions in our database, including 3 recalls and 1 clearance.

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 International Life Sciences have FDA actions?

International Life Sciences has 4 FDA actions in our database, including 3 recalls and 1 device clearance.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K260317" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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