RecallHawk

extriCARE® 1000 Negative Pressure Wound Therapy System

Alleva Medical Devices

Summary

Alleva Medical Devices received 510(k) clearance for extriCARE® 1000 Negative Pressure Wound Therapy System, a OMP device. Cleared on 2025-10-03.

Details

Source

510(k) Clearance

External ID

K251646

Action Date

2025-10-03

Status

Traditional

Category

device

Product Code

OMP

Product Description

extriCARE® 1000 Negative Pressure Wound Therapy System. Product code: OMP.

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. Alleva Medical Devices has received 2 total clearances in our database.

Alleva Medical Devices 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 Alleva Medical Devices have FDA actions?

Alleva Medical Devices 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 "K251646" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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