HYPREVENTION

FDA Device Registration & Listing · New York, NY, US · Registration 3021638889

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3021638889
FEI Number
3021638889
Entity Name
HYPREVENTION
City/State/Country
New York, NY, US
Establishment Address
1411 Broadway Fl 16, New York, NY 10018, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hyprevention (Owner Number: 10094254)
Owner / Operator Contact Address
1411 Broadway, fl16, New York, NY 10018, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K191709
PMA Number
N/A

All Registered Proprietary Names

V-STRUT V-STRUT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NDN Cement, Bone, Vertebroplasty Orthopedic Class 2 888.3027 2025-11-25
LOD Bone Cement Orthopedic Class 2 888.3027 2025-11-25
NDN Cement, Bone, Vertebroplasty Orthopedic Class 2 888.3027 2025-11-20
LOD Bone Cement Orthopedic Class 2 888.3027 2025-11-20

Official Correspondent

Cecile Vienney Vivez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hyprevention
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021638889. Last updated year: 2026. Please use registration number 3021638889 when referencing this establishment in official correspondence.
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