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Bio2 Technologies 1000063

by BIO2 Technologies, Inc.

Bio2 Technologies 1000063 is a Class II device made by BIO2 Technologies, Inc., listed in FDA GUDID since 20 Oct 2015 (UDI-DI B01010000631), 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 NumberB01010000631 UDI-DI Date20 Oct 2015ListedStatusListed 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  • Withdrawn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
Bio2 Technologies
Generic name
Synthetic bone graft
Model / reference
1000063
Description
VITRIUM C LARGE, 6 x 23
Primary DI / UDI-DI
B01010000631
FDA product code
MQV, OIS
GMDN term
Synthetic bone graft
Device class
Class II
Regulation number
888.3045
GUDID distribution status
In Commercial Distribution

Related devices

Category: Synthetic bone graft

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Other devices filed under Synthetic bone graft.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)