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Sveltiva 005-00036

by Cao Group, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00872320007218 UDI-DI Date1 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Sveltiva
Generic Name
Multi-modality skin/body contouring system
Model / Reference
005-00036
Primary DI / UDI-DI
00872320007218
FDA Product Code
PBX, OHV
GMDN Term
Multi-modality skin/body contouring system
Device Class
Class II
Regulation Number
878.4400, 878.4590
GUDID distribution status
In Commercial Distribution

Other devices from Cao Group, Inc.

See all devices from Cao Group, Inc. →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No