FDA UDI In Commercial Distribution 🇺🇸 United States

VySpan™

DI: 00840283403262 · Model: 05-TC-R40 · VY SPINE LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VySpan™
Primary DI
00840283403262
Version / Model
05-TC-R40
Company Name
VY SPINE LLC
Labeler DUNS
049592888
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-16
Public Version
1
Public Version Date
2026-04-24
Public Version Status
New
Public Device Record Key
21b986e7-1fa5-4a71-b83a-4d7e5c2d34be

Device Description

Reduction Screw Caddy

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 Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKG Posterior Cervical Screw System
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
67309 Spinal fixation implant/sterilization container set

Identifiers

Type ID
Primary 00840283403262

Customer Contacts

Phone
866-489-7746

Premarket Submissions

Submission Number Supplement Number
K213394 000