Braun Silk.expert Pro 3 PL3020

by Procter & Gamble Manufacturing Company, the

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00069055132104 UDI-DI	Date8 Sep 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Braun Silk.expert Pro 3
Generic Name: Home-use intense pulsed light hair removal unit
Model / Reference: PL3020

Primary DI / UDI-DI: 00069055132104
FDA Product Code: GEX, OHT
GMDN Term: Home-use intense pulsed light hair removal unit

Device Class: Class II
Regulation Number: 878.4810
GUDID distribution status: In Commercial Distribution

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Properties

Over-the-Counter
Convenience Kit
Serial Number
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No