FDA UDI In Commercial Distribution 🇺🇸 United States

FlareHawk

DI: 03662663094573 · Model: FHPAXT0923H · Highridge Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FlareHawk
Primary DI
03662663094573
Version / Model
FHPAXT0923H
Catalog Number
FHPAXT0923H
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-03
Public Version
2
Public Version Date
2026-03-20
Public Version Status
Update
Public Device Record Key
e0ce80fe-232c-4e5e-89fb-e6579cb8b995

Device Description

Shell, Lordotic Xtra Tall 25 mm, FlareHawk 9

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 03662663094573

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182114 000