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Osteoboost Small

by Bone Health Technologies, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860003039724 UDI-DIDate12 Oct 2024ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Osteoboost
Generic Name
Circulatory/musculoskeletal vibration therapy unit, hand-held
Model / Ref / Catalog
Small, FGN-09-3002
Primary DI / UDI-DI
00860003039724
De Novo Number
FDA Product Code
QZO
GMDN Term
Circulatory/musculoskeletal vibration therapy unit, hand-held
Device Class
Class II
Regulation Number
888.5895
GUDID distribution status
Not in Commercial Distribution

Other devices from Bone Health Technologies, Inc.

  • Osteoboost Belt

    Class II

Properties

  • Prescription Use

Other properties (13)

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