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Orthofix Osteogenesis Stimulator 3202D

by Orthofix US LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number18257200080687 UDI-DI Date12 May 2015ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Orthofix Osteogenesis Stimulator
Generic Name
Patient-worn bone growth electromagnetic stimulator
Model / Ref / Catalog
3202D, 653202-0018
Primary DI / UDI-DI
18257200080687
PMA Number
FDA Product Code
LOF
GMDN Term
Patient-worn bone growth electromagnetic stimulator
Device Class
Class II
Regulation Number
890.5870
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient-worn bone growth electromagnetic stimulator

Cleared under the same submission (P850007)

Show all (12)

Other devices from Orthofix US LLC

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Properties

  • Single Use
  • Prescription Use
  • Serial Number

Other properties (11)

  • Sterile: 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
  • Expiration Date: No
  • Manufacturing Date: No