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ScrewPlant® Zirconia Abutment Base 1037-30CB

by Implant Direct Sybron Manufacturing LLC

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 Number10841307115281 UDI-DI Date14 Sep 2015ListedStatusListed 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  • Withdrawn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

Trade Name
ScrewPlant® Zirconia Abutment Base
Generic Name
Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog
1037-30CB
Primary DI / UDI-DI
10841307115281
GMDN Term
Dental implant suprastructure, permanent, preformed
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Implant Direct Sybron Manufacturing LLC

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Properties

  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number

Other properties (9)

  • Sterile: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No