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Simplant 37473

by Dentsply Implants Manufacturing GmbH

Simplant 37473 is a Class I device made by Dentsply Implants Manufacturing GmbH, listed in FDA GUDID since 26 Feb 2025 (UDI-DI 07392532290466), 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 Number07392532290466 UDI-DI Date26 Feb 2025ListedStatusListed 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  • Withdrawn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
Dental implantation drilling template, custom-made
Model / Ref / Catalog
37473
Primary DI / UDI-DI
07392532290466
FDA product code
NDP
GMDN term
Dental implantation drilling template, custom-made
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental implantation drilling template, custom-made

Other devices from Dentsply Implants Manufacturing GmbH

See all devices from Dentsply Implants Manufacturing GmbH →

Properties

  • Single use
  • Lot / batch number
Other properties (13, all answered No)