RecallHawk

Super Upper Limbs Versalock Plating System

GM Dos Reis Industria e Comercio Ltda.

Summary

GM Dos Reis Industria e Comercio Ltda. received 510(k) clearance for Super Upper Limbs Versalock Plating System, a HRS device. Cleared on 2026-03-17.

Details

Source

510(k) Clearance

External ID

K260390

Action Date

2026-03-17

Status

Traditional

Category

device

Product Code

HRS

Product Description

Super Upper Limbs Versalock Plating System. Product code: HRS.

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. GM Dos Reis Industria e Comercio Ltda. has received 11 total clearances in our database.

GM Dos Reis Industria e Comercio Ltda. has 11 FDA actions in our database, including 11 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 GM Dos Reis Industria e Comercio Ltda. have FDA actions?

GM Dos Reis Industria e Comercio Ltda. has 11 FDA actions in our database, including 0 recalls and 11 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K260390" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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