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Aveli AVE001

by Revelle Aesthetics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850036790006 UDI-DI Date14 Feb 2022ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Aveli
Generic Name
Cellulite fibrous tether manual cutter
Model / Reference
AVE001
Primary DI / UDI-DI
00850036790006
510(k) Number
FDA Product Code
GDI, FTD, OUP
GMDN Term
Cellulite fibrous tether manual cutter
Device Class
Class I
Regulation Number
878.4800, 878.4580, 878.4790
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cellulite fibrous tether manual cutter

Cleared under the same submission (K212399)

Cleared under the same submission (K221336)

Cleared under the same submission (K232153)

Similar devices

Also classified as Cellulite fibrous tether manual cutter.

Other devices from Revelle Aesthetics, Inc.

  • Aveli AVE002

    Class II

  • Alite AVE003

    Class II

  • Avéli

    Class II

  • Avéli

    Class II

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No