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Sciograft Sg-250-S

by Odontit S.A.

Sciograft Sg-250-S is a Class II device made by Odontit S.A., listed in FDA GUDID since 27 Feb 2024 (UDI-DI D914SG250S0), 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 NumberD914SG250S0 UDI-DI Date27 Feb 2024ListedStatusListed 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  • Withdrawn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
Sciograft
Generic name
Dental bone void filling material, animal-derived
Model / reference
SG-250-S
Primary DI / UDI-DI
D914SG250S0
FDA product code
NPM
GMDN term
Dental bone void filling material, animal-derived
Device class
Class II
Regulation number
872.3930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental bone matrix implant, animal-derived

Similar devices in this category

Other devices filed under Dental bone matrix implant, animal-derived.

Other devices from Odontit S.A.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)