FDA UDI In Commercial Distribution 🇺🇸 United States

HyperFlex® Bunion Correction System

DI: G559HF2131LFT0 · Model: HF-2131-LFT · HYPERFLEX MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HyperFlex® Bunion Correction System
Primary DI
G559HF2131LFT0
Version / Model
HF-2131-LFT
Company Name
HYPERFLEX MEDICAL INC.
Labeler DUNS
119512231
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-01
Public Version
1
Public Version Date
2026-01-09
Public Version Status
New
Public Device Record Key
9de82e8b-f2c8-4834-b8f4-2b7e7a903c15

Device Description

Hyperflex Small-Large-Left - Titanium

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRS Plate, Fixation, Bone

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary G559HF2131LFT0

Premarket Submissions

Submission Number Supplement Number
K252997 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Small-Large-Left