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UltraClear AS-BM-00055

by Acclaro Corporation

UltraClear AS-BM-00055 is a Class II device made by Acclaro Corporation, listed in FDA GUDID since 11 Feb 2022 (UDI-DI 00850039149047), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850039149047 UDI-DI Date11 Feb 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  • Withdrawn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
UltraClear
Generic name
Dermatological solid-state laser system
Model / reference
AS-BM-00055
Primary DI / UDI-DI
00850039149047
FDA product code
GEX
GMDN term
Dermatological solid-state laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dermatological solid-state laser system

Similar devices in this category

Other devices filed under Dermatological solid-state laser system.

Other devices from Acclaro Corporation

See all devices from Acclaro Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)