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BioHorizons 400-260

by Biohorizons Implant Systems Inc.

BioHorizons 400-260 is a Class II device made by Biohorizons Implant Systems Inc., listed in FDA GUDID since 21 Sep 2015 (UDI-DI 00847236010249), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00847236010249 UDI-DI Date21 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
BioHorizons
Generic name
Craniofacial bone tack, non-bioabsorbable
Model / reference
400-260
Primary DI / UDI-DI
00847236010249
FDA product code
DZL
GMDN term
Craniofacial bone tack, non-bioabsorbable
Device class
Class II
Regulation number
872.4880
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental regeneration membrane fixation tack, non-bioabsorbable

Similar devices

Other devices filed under FDA product code DZL (Screw, Fixation, Intraosseous).

Other devices from Biohorizons Implant Systems Inc.

See all devices from Biohorizons Implant Systems Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)