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Osung Mnd CSCOM5

by Osung Mnd Co., Ltd.

Osung Mnd CSCOM5 is a Class I device made by Osung Mnd Co., Ltd., listed in FDA GUDID since 4 Mar 2024 (UDI-DI 08800075609472), 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 Number08800075609472 UDI-DI Date4 Mar 2024ListedStatusListed 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  • Withdrawn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
Osung Mnd
Generic name
Dental material application tool, reusable
Model / reference
CSCOM5
Primary DI / UDI-DI
08800075609472
FDA product code
EIY
GMDN term
Dental material application tool, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code EIY (Instrument, Filling, Plastic, Dental).

Other devices from Osung Mnd Co., Ltd.

See all devices from Osung Mnd Co., Ltd. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)