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TheraClear

FDA UDI

Class II (US FDA UDI)

by Theravant Corporation

Identity

Trade Name
TheraClear FDA UDI
Generic Name
Multi-modality skin surface treatment system generator FDA UDI
Model / Reference
30TC03000AA FDA UDI

Identifiers

Catalog Number
30TC030 FDA UDI
Primary DI / UDI-DI
B30530TC0300 FDA UDI
FDA Product Code
ONF FDA UDI
GMDN Term
Multi-modality skin surface treatment system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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: Multi-modality skin surface treatment system generator

TheraClear by Theravant Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 79202d4a-7ecb-46d5-b539-02c1a1eb3c1c 33 fields · synced May 31, 2026