← Back to catalogue

Vaser

FDA UDI

Class II (US FDA UDI)

by Solta Medical, Inc.

Identity

Trade Name
VASER FDA UDI
Generic Name
Ultrasonic skin/body contouring system FDA UDI
Device Name
Liposonix System Model 2, Refurbished FDA UDI
Model / Reference
P005999R FDA UDI
Description
Liposonix System Model 2, Refurbished FDA UDI

Identifiers

Catalog Number
P005999R FDA UDI
Primary DI / UDI-DI
00816995027027 FDA UDI
FDA Product Code
OHV FDA UDI
GMDN Term
Ultrasonic skin/body contouring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4590 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultrasonic skin/body contouring system

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

Similar devices

Also classified as Ultrasonic skin/body contouring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Solta Medical, Inc.

Sources (1)

  • FDA UDI 3d55a2d5-f505-4d66-8f4a-093fcd84d7b7 34 fields · synced May 30, 2026