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NA surgically Invasive Instruments

by Institut Straumann SA 183 variants

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

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 Number07630031713155 UDI-DI Date22 Sep 2023ListedStatusListed GUDID: 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  • Withdrawn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/maxillofacial surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
surgically Invasive Instruments, 026.0052S
Primary DI / UDI-DI
07630031713155
FDA Product Code
NDP
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, single-use
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution
Size
Length — 33 Millimeter
Outer Diameter — 4.8 Millimeter

Related devices

Category: Dental/maxillofacial surgical procedure kit, non-medicated, single-use

Other devices from Institut Straumann SA

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No