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NA Non-invasive Instruments

by Institut Straumann SA 54 variants

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07630031727459 UDI-DI Date30 Sep 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Dental implant x-ray template
Model / Ref / Catalog
Non-invasive Instruments, 150.230
Primary DI / UDI-DI
07630031727459
FDA Product Code
NDP
GMDN Term
Dental implant x-ray template
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Dental implant x-ray template

Other devices from Institut Straumann SA

See all devices from Institut Straumann SA →

Properties

  • Prescription Use
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No