← Back to catalogue

LB2 + LF2 kit

FDA UDI

Class II (US FDA UDI)

by Venus Concept Inc.

Identity

Trade Name
LB2 + LF2 kit FDA UDI
Generic Name
Radio-frequency skin contouring system applicator, bipolar FDA UDI
Device Name
Venus Legacy LB2 and LF2 applicators package for shipment. FDA UDI
Model / Reference
PK000039 FDA UDI
Description
Venus Legacy LB2 and LF2 applicators package for shipment. FDA UDI

Identifiers

Primary DI / UDI-DI
07290016540062 FDA UDI
510(k) Number
K143554 FDA UDI
K191528 FDA UDI
FDA Product Code
PBX FDA UDI
GEI FDA UDI
GMDN Term
Radio-frequency skin contouring system applicator, bipolar FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radio-frequency skin contouring system applicator, bipolar

LB2 + LF2 kit by Venus Concept Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin contouring system applicator, bipolar.

Cleared under the same submission

K143554 also covers:

K191528 also covers:

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
Venus Concept Inc.

Sources (1)

  • FDA UDI ad92d90b-c6fb-424b-b1b5-24310a1a16d7 34 fields · synced May 31, 2026