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Simplant Version 18

by Dentsply Implants NV 2 variants

Simplant Version 18 (54500277P18) is a Class II device made by Dentsply Implants NV, listed in FDA GUDID since 1 May 2018 (UDI-DI 07392532191251), 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 Number07392532191251 UDI-DI Date1 May 2018ListedStatusListed 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  • Withdrawn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, 54500277P18
Primary DI / UDI-DI
07392532191251
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

Similar devices

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

Other devices from Dentsply Implants NV

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Properties

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