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Legend Pro

FDA UDI

Class II (US FDA UDI)

by Pollogen Ltd

Identity

Trade Name
Legend Pro FDA UDI
Generic Name
Radio-frequency skin surface treatment system applicator FDA UDI
Device Name
LP APPLICATOR 3 Applicators 1-3 provide RF energy that heats biological tissue in a controlled fashion for non-ablative therapeutic effects. Non ablative effects are used to trigger collagen remodeling for the treatment of wrinkles and rhytides. Applicator No. 1 is indicated for the treatment of large facial areas. It is connected to the main unit by a cable containing electrical wiring and a connector, consists of a plastic body with an integrated electronic system, 6 electrodes and indication light guide ring. FDA UDI
Model / Reference
Legend Pro FDA UDI
Description
LP APPLICATOR 3 Applicators 1-3 provide RF energy that heats biological tissue in a controlled fashion for non-ablative therapeutic effects. Non ablative effects are used to trigger collagen remodeling for the treatment of wrinkles and rhytides. Applicator No. 1 is indicated for the treatment of large facial areas. It is connected to the main unit by a cable containing electrical wiring and a connector, consists of a plastic body with an integrated electronic system, 6 electrodes and indication light guide ring. FDA UDI

Identifiers

Catalog Number
20900320 FDA UDI
Primary DI / UDI-DI
07290016586169 FDA UDI
510(k) Number
K173503 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Radio-frequency skin surface treatment system applicator 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

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: Radio-frequency skin surface treatment system applicator

Legend Pro by Pollogen Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin surface treatment system applicator.

Cleared under the same submission

K173503 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pollogen Ltd

Sources (1)

  • FDA UDI cdd6c40b-9df3-4344-9170-02975e432b5d 35 fields · synced May 29, 2026