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Curette 7439-20

by Koros USA, Inc.

Curette 7439-20 is a Class I device made by Koros USA, Inc., listed in FDA GUDID since 1 Feb 2022 (UDI-DI 10840199527127), 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 Number10840199527127 UDI-DI Date1 Feb 2022ListedStatusListed 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  • Withdrawn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
Curette
Generic name
General-purpose curette
Model / Ref / Catalog
7439-20
Primary DI / UDI-DI
10840199527127
FDA product code
FZS
GMDN term
General-purpose curette
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusableGeneral-purpose curetteOphthalmic curette, reusable

Similar devices in this category

Other devices filed under Ophthalmic curette, reusable.

Other devices from Koros USA, Inc.

See all devices from Koros USA, Inc. →

Properties

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