FDA UDI In Commercial Distribution 🇺🇸 United States

Biomet OrthoPak Non-invasive Bone Growth Stimulator System

DI: 00812301020249 · Model: 1067719 · EBI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Biomet OrthoPak Non-invasive Bone Growth Stimulator System
Primary DI
00812301020249
Version / Model
1067719
Catalog Number
1067719
Company Name
EBI, LLC
Labeler DUNS
050410323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-19
Public Version
7
Public Version Date
2025-05-23
Public Version Status
Update
Public Device Record Key
a35950d7-39bd-4a2e-804a-bd033cb20812

Device Description

ORTHOPAK STIMULATOR, BIOMET

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LOF Stimulator, Bone Growth, Non-Invasive

GMDN Terms

Code Name
35463 Patient-worn bone growth electromagnetic stimulator

Identifiers

Type ID
Primary 00812301020249

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P850022 017