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Lotus Plus DS LPHM22-2-1345

by Ortho Technology, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00190730028563 UDI-DIDate3 May 2019ListedStatusListed GUDID: not 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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Trade Name
Lotus Plus DS
Generic Name
Orthodontic bracket, metal
Model / Reference
LPHM22-2-1345
Primary DI / UDI-DI
00190730028563
FDA Product Code
EJF
GMDN Term
Orthodontic bracket, metal
Device Class
Class I
Regulation Number
872.5410
GUDID distribution status
Not in Commercial Distribution

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See all devices from Ortho Technology, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

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