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SPP Device, Dermalinfusion A0029

by Zeltiq Aesthetics, Inc.

SPP Device, Dermalinfusion A0029 is a Class I device made by Zeltiq Aesthetics, Inc., listed in FDA GUDID since 30 Apr 2021 (UDI-DI 00816417022432), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816417022432 UDI-DI Date30 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SPP Device, Dermalinfusion
Generic name
Dermabrasion brush, rotary
Model / Ref / Catalog
A0029
Primary DI / UDI-DI
00816417022432
FDA product code
GFE
GMDN term
Dermabrasion brush, rotary
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dermabrasion brush, rotary

Similar devices

Other devices filed under FDA product code GFE (Brush, Dermabrasion, Powered).

Other devices from Zeltiq Aesthetics, Inc.

See all devices from Zeltiq Aesthetics, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)