TheraFace

FDA UDI

Class II (US FDA UDI)

by Therabody, Inc.

Identity

Trade Name: TheraFace FDA UDI
Generic Name: Blue/red/infrared phototherapy lamp FDA UDI
Device Name: The TheraFace PRO is a 4-in-1 handheld device that takes facial wellness to the next level by helping to reduce tension, relax facial muscles, and achieve healthier-looking skin by gently stimulating the face. It includes microcurrent, blue, red, and red+infrared light LED, and cleansing treatments, allowing you to customize your facial therapy in one easy-to-use versatile device. Use the variety of treatment rings to help lift, tone, rejuvenate, and deep clean. FDA UDI
Model / Reference: TheraFace PRO Black FDA UDI
Description: The TheraFace PRO is a 4-in-1 handheld device that takes facial wellness to the next level by helping to reduce tension, relax facial muscles, and achieve healthier-looking skin by gently stimulating the face. It includes microcurrent, blue, red, and red+infrared light LED, and cleansing treatments, allowing you to customize your facial therapy in one easy-to-use versatile device. Use the variety of treatment rings to help lift, tone, rejuvenate, and deep clean. FDA UDI

Identifiers

Primary DI / UDI-DI: 00810036056724 FDA UDI
FDA Product Code: ILY FDA UDI
IRO FDA UDI
NFO FDA UDI
OHS FDA UDI
OLP FDA UDI
GMDN Term: Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5500 FDA UDI
890.5975 FDA UDI
882.5890 FDA UDI
878.4810 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

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Blue/red/infrared phototherapy lamp Transcutaneous electrical stimulation probe

TheraFace by Therabody, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Transcutaneous electrical stimulation probe.

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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 II	Pending data

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Manufacturer

Manufacturer: Therabody, Inc.

Sources (1)

FDA UDI 463306b9-d876-49a1-9e04-b88f8476ef87 33 fields · synced May 30, 2026