Data / Medical devices / United States / Secada Medical, LLC D.B.A Ventris Medical
Secada Medical, LLC D.B.A Ventris Medical: FDA-registered device maker in Newport Beach, CA, United States, 4 510(k) clearances
Secada Medical, LLC D.B.A Ventris Medical is registered with the FDA (registration 3014078231) in Newport Beach, CA, United States. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 2, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3014078231
- Address
- 1201 Dove Street Suite 470, Newport Beach, CA, United States, 92660
- Owner or operator
- Secada Medical, LLC d.b.a Ventris Medical (10087455)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- March 1, 2023
- Registered through
- 2026
- Brand names listed
- Amplify, Backpack AF Osteoinductive Bone Graft, Connext Surgical Matrix
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Filler, Bone Void, Calcium Compound | MQV | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | MBP | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Wound Dressing With Animal-Derived Material(S) | KGN | U | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 2, 2026 | K260596 | Collagen Wound Powder | KGN | Substantially Equivalent | Ventris Medical | accessdata.fda.gov |
| March 21, 2025 | K250556 | Porous Biologic Scaffold | MQV | Substantially Equivalent | Ventris Medical | accessdata.fda.gov |
| March 7, 2024 | K240458 | Synthetic Bone Putty | MQV | Substantially Equivalent | Ventris Medical | accessdata.fda.gov |
| September 2, 2022 | K221644 | Synthetic Bone Putty | MQV | Substantially Equivalent | Ventris Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Wound Dressing With Animal-Derived Material(S)
- All makers of Filler, Bone Void, Calcium Compound
- All makers of Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Updated July 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.