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Aveli AVE002

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 Number00850036790013 UDI-DI Date26 Feb 2024ListedStatusListed 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  • Withdrawn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
AVE002
Primary DI / UDI-DI
00850036790013
510(k) Number
FDA Product Code
OUP, GDI, FTD
GMDN Term
Cellulite fibrous tether manual cutter
Device Class
Class II
Regulation Number
878.4790, 878.4800, 878.4580
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.

  • Alite AVE003

    Class II

  • Aveli AVE001

    Class I

  • 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