Skip to content

Mirabay Nlpu-002

by Mirabay Orthodontics Corporation

Mirabay Nlpu-002 is a Class I device made by Mirabay Orthodontics Corporation, listed in FDA GUDID since 3 Feb 2025 (UDI-DI 05061075025836), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05061075025836 UDI-DI Date3 Feb 2025ListedStatusListed 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  • Withdrawn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
Mirabay
Generic name
Orthodontic inter-arch elastic band
Model / Ref / Catalog
NLPU-002
Primary DI / UDI-DI
05061075025836
FDA product code
ECI
GMDN term
Orthodontic inter-arch elastic band
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic inter-arch elastic band

Other devices from Mirabay Orthodontics Corporation

See all devices from Mirabay Orthodontics Corporation →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)