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Reflex Nickel Titanium Wire 381-271

by Tp Orthodontics, Inc.

Reflex Nickel Titanium Wire 381-271 is a Class I device made by Tp Orthodontics, Inc., listed in FDA GUDID since 15 Mar 2021 (UDI-DI 00192029031193), 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 Number00192029031193 UDI-DI Date15 Mar 2021ListedStatusListed 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  • Withdrawn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
Reflex Nickel Titanium Wire
Generic name
Orthodontic wire
Model / reference
381-271
Description
Standard Arch Form Upper Rectangular
Primary DI / UDI-DI
00192029031193
FDA product code
DZC
GMDN term
Orthodontic wire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic wire

Similar devices in this category

Other devices filed under Orthodontic wire.

Other devices from Tp Orthodontics, Inc.

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)