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Leone Spa

FDA UDI

Class I (US FDA UDI)

by Leone Spa

Identity

Trade Name
LEONE SPA FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
STANDARD BITE HARD S/STEEL 0,5mm FDA UDI
Model / Reference
A0720-00 FDA UDI
Description
STANDARD BITE HARD S/STEEL 0,5mm FDA UDI

Identifiers

Catalog Number
A0720-00 FDA UDI
Primary DI / UDI-DI
08033707000785 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic retainer

Leone Spa by Leone Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Leone Spa

Sources (1)

  • FDA UDI cebb0b06-e19c-4f3e-aad7-f4e4cc848723 34 fields · synced May 30, 2026