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Screwdriver 353-01

by Neurovention LLC

Screwdriver 353-01 is a Class I device made by Neurovention LLC, listed in FDA GUDID since 21 Jun 2022 (UDI-DI G28435301), 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 NumberG28435301 UDI-DI Date21 Jun 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Screwdriver
Generic name
Surgical screwdriver, reusable
Model / reference
353-01
Primary DI / UDI-DI
G28435301
FDA product code
GXL, HAO
GMDN term
Surgical screwdriver, reusable
Device class
Class I
Regulation number
882.4900, 882.4535
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical screwdriver, reusable

Other devices from Neurovention LLC

See all devices from Neurovention LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)