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Leona

FDA UDI

Class II (US FDA UDI)

by Loon Lab Inc.

Identity

Trade Name
LEONA FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
A menstrual cup is feminine hygiene product that collects the menstrual fluid during menstruation. FDA UDI
Model / Reference
LEONA BASIC SMALL FDA UDI
Description
A menstrual cup is feminine hygiene product that collects the menstrual fluid during menstruation. FDA UDI

Identifiers

Primary DI / UDI-DI
08809599750059 FDA UDI
FDA Product Code
HHE FDA UDI
GMDN Term
Menstrual cup/disc, non-latex, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Menstrual cup/disc, non-latex, reusable

Leona by Loon Lab Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual cup/disc, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Loon Lab Inc.

Sources (1)

  • FDA UDI 03e2f0e9-10a1-41d6-95ca-ab3558d3924d 33 fields · synced Jun 1, 2026