← Back to catalogue

Origins

FDA UDI

Class II (US FDA UDI)

by Solta Medical, Inc.

Identity

Trade Name
ORIGINS FDA UDI
Generic Name
Liposuction system FDA UDI
Device Name
4.6 MM, SST-6, 34 CM FDA UDI
Model / Reference
130-0101 FDA UDI
Description
4.6 MM, SST-6, 34 CM FDA UDI

Identifiers

Catalog Number
130-0101 FDA UDI
Primary DI / UDI-DI
00816995020714 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Liposuction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system

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

Similar devices

Also classified as Liposuction 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 2da2f0f4-1e98-4927-a93e-5adf17baab04 34 fields · synced Jun 6, 2026