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Neoss Implant System 90230

by Neoss, Ltd.

Neoss Implant System 90230 is a Class I device made by Neoss, Ltd., listed in FDA GUDID since 20 Feb 2017 (UDI-DI 05060440333408), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number05060440333408 UDI-DI Date20 Feb 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Neoss Implant System
Generic name
Dental precision attachment fitting/adjustment tool
Model / Ref / Catalog
90230
Primary DI / UDI-DI
05060440333408
FDA product code
NDP
GMDN term
Dental precision attachment fitting/adjustment tool
Device class
Class I
Regulation number
872.3980
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Neoss, Ltd.

See all devices from Neoss, Ltd. →

Properties

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