Philips 220592

by Sbo Hearing A/S

Philips 220592 is a hearing aid/implant system remote control (FDA Class II) made by Sbo Hearing A/S, listed in FDA GUDID since 16 Dec 2020 (UDI-DI 05714464011292), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05714464011292 UDI-DI	Date16 Dec 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05714464011292

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Philips
Generic name: Hearing aid/implant system remote control
Model / reference: 220592

Primary DI / UDI-DI: 05714464011292
FDA product code: KLW, OSM
GMDN term: Hearing aid/implant system remote control

Device class: Class II
Regulation number: 874.3400, 874.3305
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

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Properties

Prescription use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)