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Neoss Implant System 90132

by Neoss, Ltd.

Neoss Implant System 90132 is a Class I device made by Neoss, Ltd., listed in FDA GUDID since 21 Feb 2017 (UDI-DI 05060440333248), 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 Number05060440333248 UDI-DI Date21 Feb 2017ListedStatusListed 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  • Withdrawn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
Surgical screwdriver, reusable
Model / Ref / Catalog
90132
Primary DI / UDI-DI
05060440333248
FDA product code
NDP
GMDN term
Surgical screwdriver, reusable
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical screwdriver, reusable

Similar devices in this category

Other devices filed under Surgical screwdriver, reusable.

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)