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LuxaPrint Ortho NX 405 nm 171626

by DMG Digital Enterprises SE GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD9821716261 UDI-DIDate26 May 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  • Withdrawn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 NX 405 nm
Generic Name
Dental appliance fabrication material, resin
Model / Ref / Catalog
171626
Primary DI / UDI-DI
D9821716261
FDA Product Code
DYT
GMDN Term
Dental appliance fabrication material, resin
Device Class
Class I
Regulation Number
872.5525
GUDID distribution status
In Commercial Distribution

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Properties

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

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Manufacturing Date: No