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Neoss Implant System 90106

by Neoss, Ltd.

Neoss Implant System 90106 is a Class II device made by Neoss, Ltd., listed in FDA GUDID since 20 Dec 2016 (UDI-DI 05060440333125), 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 Number05060440333125 UDI-DI Date20 Dec 2016ListedStatusListed 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  • Withdrawn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
Neoss Implant System
Generic name
Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog
90106
Primary DI / UDI-DI
05060440333125
FDA product code
NHA
GMDN term
Dental implant suprastructure, permanent, preformed
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant suprastructure, permanent, preformed

Similar devices in this category

Other devices filed under Dental implant suprastructure, permanent, preformed.

Other devices from Neoss, Ltd.

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Properties

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