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Luxisse 0

by Heany Industries, Inc. 58 variants

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817724029022 UDI-DI Date31 Jul 2023ListedStatusListed 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  • Withdrawn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
Luxisse
Generic Name
Dental appliance fabrication material, ceramic
Model / Ref / Catalog
0, MDDK3701ZF10B2
Primary DI / UDI-DI
00817724029022
FDA Product Code
EIH
GMDN Term
Dental appliance fabrication material, ceramic
Device Class
Class II
Regulation Number
872.6660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental appliance fabrication material, ceramic

Other devices from Heany Industries, Inc.

See all devices from Heany Industries, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No