Neoss Implant System 90113

Neoss Implant System 90113 is a Class I device made by Neoss, Ltd., listed in FDA GUDID since 10 Jan 2017 (UDI-DI 05060440333170), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05060440333170 UDI-DI	Date10 Jan 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05060440333170

Coverage

1 jurisdiction

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Withdrawn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: 90113

Primary DI / UDI-DI: 05060440333170
FDA product code: EGG
GMDN term: Dental implant suprastructure, permanent, preformed

Device class: Class I
Regulation number: 872.3165
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Single use
Implantable
Prescription use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (8, all answered No)