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Simplant Version 18.5

by Dentsply Implants NV

Simplant Version 18.5 (54500277V185) is a Class II device made by Dentsply Implants NV, listed in FDA GUDID since 25 Apr 2019 (UDI-DI 07392532208416), 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 Number07392532208416 UDI-DI Date25 Apr 2019ListedStatusListed 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  • Withdrawn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
Simplant
Generic name
Panoramic/tomographic dental x-ray system application software
Model / Ref / Catalog
Version 18.5, 54500277V185
Primary DI / UDI-DI
07392532208416
FDA product code
LLZ
GMDN term
Panoramic/tomographic dental x-ray system application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Panoramic/tomographic dental x-ray system application software

Similar devices

Other devices filed under FDA product code LLZ (System, image processing, radiological).

Other devices from Dentsply Implants NV

See all devices from Dentsply Implants NV →

Properties

  • Prescription use
  • Manufacturing date
Other properties (13, all answered No)