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Mirabay 811-0001

by Mirabay Orthodontics Corporation

Mirabay 811-0001 is a Class I device made by Mirabay Orthodontics Corporation, listed in FDA GUDID since 3 Feb 2025 (UDI-DI 05061075025348), 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 Number05061075025348 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  • Withdrawn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 pliers
Model / Ref / Catalog
811-0001
Primary DI / UDI-DI
05061075025348
FDA product code
JEX
GMDN term
Orthodontic pliers
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthodontic pliers

Other devices from Mirabay Orthodontics Corporation

See all devices from Mirabay Orthodontics Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)