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Transform (T3 Applicator) AG609899A

by Inmode MD, Ltd.

Transform (T3 Applicator) AG609899A is a Class II device made by Inmode MD, Ltd., listed in FDA GUDID since 27 Oct 2022 (UDI-DI 07290016633689), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290016633689 UDI-DI Date27 Oct 2022ListedStatusListed 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  • Withdrawn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
Transform (T3 Applicator)
Generic name
Radio-frequency skin surface treatment system applicator
Model / Ref / Catalog
AG609899A
Primary DI / UDI-DI
07290016633689
FDA product code
IPF, PBX, GJZ
GMDN term
Radio-frequency skin surface treatment system applicator
Device class
Class II
Regulation number
890.5850, 878.4400, 864.7500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radio-frequency skin surface treatment system applicator

Other devices from Inmode MD, Ltd.

See all devices from Inmode MD, Ltd. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)