FDA UDI In Commercial Distribution 🇺🇸 United States

VerteGlide Spinal Growth Guidance System

DI: 00840194480222 · Model: 01-1720-0500 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VerteGlide Spinal Growth Guidance System
Primary DI
00840194480222
Version / Model
01-1720-0500
Catalog Number
01-1720-0500
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-31
Public Version
1
Public Version Date
2025-04-08
Public Version Status
New
Public Device Record Key
52cf07d0-76d9-489b-b42d-aef62e638cc4

Device Description

VERTEGLIDE PROVISIONAL SET SCREW DRIVER

Device Characteristics

Single Use
No
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
Yes
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
HXX SCREWDRIVER

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 00840194480222

Customer Contacts