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Wide Platform Multi-Im Esthetic Abutment Laboratory Scan Body Kit Sbltzmipa

by Biotechnology Institute Sl GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08435389818212 UDI-DIDate11 Nov 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Wide Platform Multi-Im Esthetic Abutment Laboratory Scan Body Kit
Generic Name
Dental implant suprastructure, temporary, preformed, reusable
Model / Reference
SBLTZMIPA
Primary DI / UDI-DI
08435389818212
FDA Product Code
NDP
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental implant suprastructure, temporary, preformed, reusable

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Properties

  • Implantable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

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