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Orthodontic Brackets

by Leone S.P.A. 1,000+ variants

Ref F2113R03

Orthodontic Brackets (F2113R03) is a device classified as Class IIa in the EU and Class I in the US made by Leone S.P.A., registered in EUDAMED on 15 Apr 2026 (Basic UDI-DI B-08033707039068) and listed in FDA GUDID since 25 Nov 2020 (UDI-DI 08033707039068), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-08033707039068 Basic UDI-DI 08033707039068UDI-DIDate15 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08033707039068 UDI-DI Date25 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08033707039068 registered 15 Apr 2026 Active
  • FDA GUDID UDI-DI 08033707039068 listed 25 Nov 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08033707039068
  2. Registered EUDAMED B-08033707039068

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Leone SpA
Generic name
Orthodontic bracket, metal
Device name
Orthodontic Brackets
Model / Ref / Catalog
F2113R03
Primary DI / UDI-DI
08033707039068
Basic UDI-DI
B-08033707039068
FDA product code
EJF
EMDN code
Q010403 Orthodontic brackets and buttons
GMDN term
Orthodontic bracket, metal
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.5410
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
IT-MF-000005986

Related devices

Category: Orthodontic tube

Similar devices in this category

Other devices filed under ORTHODONTIC BRACKETS AND BUTTONS.

Other devices from Leone S.P.A.

See all devices from Leone S.P.A. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)