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Threaded rods titanium 43007295

by bredent GmbH & Co. KG

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 NumberEBRE430072950 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: 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  • Withdrawn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
Threaded rods titanium
Generic Name
Screw endosteal dental implant, two-piece
Model / Ref / Catalog
43007295
Primary DI / UDI-DI
EBRE430072950
FDA Product Code
EBL
GMDN Term
Screw endosteal dental implant, two-piece
Device Class
Class I
Regulation Number
872.3740
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 1.8 Millimeter
Length — 8.5 Millimeter

Related devices

Category: Screw endosteal dental implant, two-piece

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Properties

  • Implantable
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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