RecallHawk

SMARTXIDE PRO

El.En S.P.A.

Summary

El.En S.P.A. received 510(k) clearance for SMARTXIDE PRO, a GEX device. Cleared on 2024-03-20.

Details

Source

510(k) Clearance

External ID

K240537

Action Date

2024-03-20

Status

Special

Category

device

Product Code

GEX

Product Description

SMARTXIDE PRO. Product code: GEX.

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. El.En S.P.A. has received 12 total clearances in our database.

El.En S.P.A. has 12 FDA actions in our database, including 12 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 El.En S.P.A. have FDA actions?

El.En S.P.A. has 12 FDA actions in our database, including 0 recalls and 12 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K240537" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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