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Evonos 130202

by Gyrus Acmi, Inc.

Evonos 130202 is a Class I device made by Gyrus Acmi, Inc., listed in FDA GUDID since 10 Sep 2018 (UDI-DI 00821925013018), 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 Number00821925013018 UDI-DI Date10 Sep 2018ListedStatusListed 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  • Withdrawn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
Evonos
Generic name
Middle ear incus hook
Model / reference
130202
Primary DI / UDI-DI
00821925013018
FDA product code
LRC
GMDN term
Middle ear incus hook
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Incus hook

Similar devices

Other devices filed under FDA product code LRC (INSTRUMENT, ENT MANUAL SURGICAL).

Other devices from Gyrus Acmi, Inc.

See all devices from Gyrus Acmi, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)