Sassy Jones

FDA UDI

Class I (US FDA UDI)

by Fgx International Inc.

Identity

Trade Name: SASSY JONES FDA UDI
Generic Name: Prescription spectacles FDA UDI
Model / Reference: 5013156-000.DQV FDA UDI

Identifiers

Primary DI / UDI-DI: 00193033464878 FDA UDI
FDA Product Code: HOI FDA UDI
GMDN Term: Prescription spectacles FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.5840 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Prescription spectacles

The SASSY JONES medical device is a Spectacle with Magnifying lenses designed to correct vision conditions such as presbyopia and refractive ametropia, providing comfortable and clear vision for individuals with eye health issues. The device features a durable spectacle frame, high-quality optical lenses, and advanced technology that enhances visual clarity and accuracy. Its user-friendly design ensures a seamless experience for wearers.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Fgx International Inc.

Sources (1)

FDA UDI 13d99e1b-3b75-47b1-aa0c-028658e5e994 33 fields · synced Jul 6, 2026