Browse hierarchy: [General, Plastic Surgery (SU)](/submissions/SU) → [Subpart E — Surgical Devices](/submissions/SU/subpart-e%E2%80%94surgical-devices) → [21 CFR 878.4820](/submissions/SU/subpart-e%E2%80%94surgical-devices/878.4820) → GFE — Brush, Dermabrasion, Powered

# GFE · Brush, Dermabrasion, Powered

_General, Plastic Surgery · 21 CFR 878.4820 · Class 1_

**Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GFE

## Overview

- **Product Code:** GFE
- **Device Name:** Brush, Dermabrasion, Powered
- **Regulation:** [21 CFR 878.4820](/submissions/SU/subpart-e%E2%80%94surgical-devices/878.4820)
- **Device Class:** 1
- **Review Panel:** [General, Plastic Surgery](/submissions/SU)

## Identification

Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.

## Classification Rationale

Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 878.9.

## Recent Cleared Devices (2 of 2)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K963204](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GFE/K963204.md) | DMS-1000C DERMOABRADER | Aesthetic Lasers, Inc. | Dec 9, 1996 | SESE |
| [K905046](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GFE/K905046.md) | DERMABRADER | Aaron Medical Industries | Dec 19, 1990 | SESE |

## Top Applicants

- Aaron Medical Industries — 1 clearance
- Aesthetic Lasers, Inc. — 1 clearance

---

**Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GFE](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GFE)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com