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LuxaPrint Ortho Plus NX 405 nm 171636

by DMG Digital Enterprises SE GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD9821716361 UDI-DIDate21 Jul 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
LuxaPrint Ortho Plus NX 405 nm
Generic Name
Dental appliance fabrication material, resin
Model / Reference
171636
Primary DI / UDI-DI
D9821716361
FDA Product Code
MQC
GMDN Term
Dental appliance fabrication material, resin
Device Class
U
GUDID distribution status
In Commercial Distribution

Other devices from DMG Digital Enterprises SE

See all devices from DMG Digital Enterprises SE →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (10)

  • 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
  • Manufacturing Date: No