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Phoenix P-300-214

by Auradonics Inc.

Phoenix P-300-214 is a Class I device made by Auradonics Inc., listed in FDA GUDID since 31 Dec 2019 (UDI-DI 00810033837722), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810033837722 UDI-DI Date31 Dec 2019ListedStatusListed 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  • Withdrawn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
Phoenix
Generic name
Orthodontic archwire/bracket ligature
Model / reference
P-300-214
Primary DI / UDI-DI
00810033837722
FDA product code
ECI
GMDN term
Orthodontic archwire/bracket ligature
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic archwire/bracket ligature

Similar devices in this category

Other devices filed under Orthodontic archwire/bracket ligature.

Other devices from Auradonics Inc.

See all devices from Auradonics Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)