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Oticon 202027

by Oticon A/S

Oticon 202027 is a Class II device made by Oticon A/S, listed in FDA GUDID since 20 Feb 2019 (UDI-DI 05707131349866), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05707131349866 UDI-DI Date20 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Oticon
Generic name
Hearing aid wireless-fitting computer-aided set
Model / reference
202027
Primary DI / UDI-DI
05707131349866
FDA product code
OSM, KLW
GMDN term
Hearing aid wireless-fitting computer-aided set
Device class
Class II
Regulation number
874.3305, 874.3400
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Hearing aid wireless-fitting computer-aided set

Similar devices

Other devices filed under FDA product code OSM (Hearing aid, air conduction with wireless technology).

Other devices from Oticon A/S

See all devices from Oticon A/S →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)