RecallHawk

G4Derm / G4Derm Plus Synthetic Wound Matrix

Gel4med, Inc.

Summary

Gel4med, Inc. received 510(k) clearance for G4Derm / G4Derm Plus Synthetic Wound Matrix, a FRO device. Cleared on 2023-10-11.

Details

Source

510(k) Clearance

External ID

K222025

Action Date

2023-10-11

Status

Traditional

Category

device

Product Code

FRO

Product Description

G4Derm / G4Derm Plus Synthetic Wound Matrix. Product code: FRO.

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.

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 Gel4med, Inc. have FDA actions?

This is the only FDA action we have on record for Gel4med, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K222025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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