FDA UDI In Commercial Distribution 🇺🇸 United States

HyperFlex® Bunion Correction System

DI: G559FB29000 · Model: FB-2900 · HYPERFLEX MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
HyperFlex® Bunion Correction System
Primary DI
G559FB29000
Version / Model
FB-2900
Company Name
HYPERFLEX MEDICAL INC.
Labeler DUNS
119512231
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-12
Public Version
1
Public Version Date
2025-06-20
Public Version Status
New
Public Device Record Key
0a440c0a-6c85-428e-813b-409cc557b1a9

Device Description

Pack:Stainless Steel:Screw Pack (SS) - 9mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary G559FB29000

Premarket Submissions

Submission Number Supplement Number
K241995 000