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Device Explorer · FDA GUDID · GMDN 32388

Dermabrasion brush, rotary

A device with wire bristles that is rotated in a power-driven tool to plane the skin (surgical removal of the epidermis and as much of the dermis as necessary) to remove scars, tattoos, pigmented nevi, fine wrinkles, or other irregularities. This is a reusable

US‑registered devices69in commercial distribution
Companies11labelers on GUDID
Single‑use16%of device records
Sterile1%labelled sterile
Prescription62%Rx‑only share
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Share of device records

Zeltiq Aesthetics, Inc.3754%
Conair Corporation913%
Healux Co.,Ltd57%
Trophy Skin, Inc46%
Neauvia North America, Inc.46%
Silhouet-Tone Corporation46%
Hichance Toys Manufacturing Limited23%
Foreo Ab11%

Top labelers

CompanyDevicesShare
Zeltiq Aesthetics, Inc.3754%
Conair Corporation913%
Healux Co.,Ltd57%
Trophy Skin, Inc46%
Neauvia North America, Inc.46%
Silhouet-Tone Corporation46%
Hichance Toys Manufacturing Limited23%
Foreo Ab11%
Canadian Pioneer Medical Technology Corporation11%
Xod Inc.11%
Cosmofrance11%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

KIWI DermaVanity Planet® Ultrasonic ScrubberVanity Planet® Microdermabrasion WandTrophy SkinZaffiro IR Treatment Body ApplicatorZaffiro SystemZaffiro WP Treatment ApplicatorZaffiro IR Treatment ApplicatorSPP Device, DermalinfusionBody Handpiece 15mmPlexus Diamond Handpiece KitStandard Diamond Handpiece KitBODY Diamond Treatment TipsDiamond Treatment TipsPlexus Pore Clarifying Handpiece KitTwist-to-Lock Waste Jar

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
GFEBrush, Dermabrasion, Powered109
GFDDermatome3
KNMDevice, Pressure Applying1

GMDN & GCC registration

  • GMDN code 32388 · non‑implantable
  • Single‑use 16% · sterile 1% · Rx‑only 62% · OTC 16%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

No closely related category with 50+ devices.

How many dermabrasion brush, rotary products are registered in the US?

69 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dermabrasion brush, rotary", from 11 companies. The largest labeler is Zeltiq Aesthetics, Inc. with 54% of records.

Which FDA product codes apply?

GFE (Brush, Dermabrasion, Powered), GFD (Dermatome), KNM (Device, Pressure Applying)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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