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Silent Scan 3300

by Avotec, Inc. 2 variants

Silent Scan 3300 is a Class II device made by Avotec, Inc., listed in FDA GUDID since 6 May 2020 (UDI-DI 00850010651095), 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 Number00850010651095 UDI-DI Date6 May 2020ListedStatusListed 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  • Withdrawn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
Silent Scan
Generic name
Patient audiovisual communication/entertainment system
Model / reference
3300
Primary DI / UDI-DI
00850010651095
FDA product code
LNH
GMDN term
Patient audiovisual communication/entertainment system
Device class
Class II
Regulation number
892.1000
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient audiovisual communication/entertainment system

Similar devices

Other devices filed under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging).

Other devices from Avotec, Inc.

See all devices from Avotec, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)