SECADA MEDICAL, LLC D.B.A VENTRIS MEDICAL

FDA Device Registration & Listing · Newport Beach, CA, US · Registration 3014078231

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
3014078231
FEI Number
3014078231
Entity Name
SECADA MEDICAL, LLC D.B.A VENTRIS MEDICAL
City/State/Country
Newport Beach, CA, US
Establishment Address
1201 Dove Street, Suite 470, Newport Beach, CA 92660, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Secada Medical, LLC d.b.a Ventris Medical (Owner Number: 10087455)
Owner / Operator Contact Address
1201 Dove Street, Suite 470, Newport Beach, CA 92660, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K221644
PMA Number
N/A

All Registered Proprietary Names

Backpack AF Osteoinductive Bone Graft Amplify Amplify

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2025-12-30
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) Orthopedic Class 2 888.3045 2025-12-30
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2024-07-26
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2023-03-01

Official Correspondent

Russell Cook

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Secada Medical, LLC d.b.a Ventris Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15
K023703 Berkeley Advanced Biomaterials, Inc. BI-OSTETIC 2003-01-30
K173933 Xenco Medical, LLC Sorrento Bioglass Bone Graft Substitute 2018-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014078231. Last updated year: 2026. Please use registration number 3014078231 when referencing this establishment in official correspondence.
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