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Thermage

FDA UDI

Class I (US FDA UDI)

by Solta Medical, Inc.

Identity

Trade Name
Thermage FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
FOOTSWITCH FDA UDI
Model / Reference
TW-1 FDA UDI
Description
FOOTSWITCH FDA UDI

Identifiers

Catalog Number
TW-1 FDA UDI
Primary DI / UDI-DI
00850608002452 FDA UDI
FDA Product Code
ISA FDA UDI
GEI FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 FDA UDI
878.4400 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

Thermage by Solta Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Solta Medical, Inc.

Sources (1)

  • FDA UDI e27dae80-7601-4e2f-9db7-1bc31a44f364 34 fields · synced Jun 8, 2026