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Atlantis® 35517

by Dentsply Ih, Inc. 2 variants

Atlantis® 35517 is a Class II device made by Dentsply Ih, Inc., listed in FDA GUDID since 3 Nov 2025 (UDI-DI 07392532213106), 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 Number07392532213106 UDI-DI Date3 Nov 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  • Withdrawn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
Atlantis®
Generic name
Dental implant suprastructure, temporary, custom-made
Model / reference
35517
Primary DI / UDI-DI
07392532213106
FDA product code
NHA
GMDN term
Dental implant suprastructure, temporary, custom-made
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Dentsply Ih, Inc.

See all devices from Dentsply Ih, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)