Alite AVE003

by Revelle Aesthetics, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00850036790020 UDI-DI	Date1 Sep 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Alite
Generic Name: Subcutaneous infusion transilluminator
Model / Reference: AVE003

Primary DI / UDI-DI: 00850036790020
FDA Product Code: FTD
GMDN Term: Subcutaneous infusion transilluminator

Device Class: Class II
Regulation Number: 878.4580
GUDID distribution status: In Commercial Distribution

Other devices from Revelle Aesthetics, Inc.

Aveli AVE002

Class II
Aveli AVE001

Class I
Avéli

Class II
Avéli

Class II

Properties

Sterile
Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number
Serial Number
Expiration Date
Manufacturing Date

Other properties (6)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No