Product code MQV: 510(k) clearances and predicates
Product code MQV covers Mg OSTEOREVIVE;Mg OSTEOCRETE. FDA lists 493 clearances under this code in the 510(k) index. This page summarizes recent clearance volume and names recent clearances by K number so you can pick predicates faster.
Clearance volume
493 clearances on file under product code MQV. Counts by year:
| Year | Clearances |
|---|---|
| 2022 | 9 |
| 2023 | 21 |
| 2024 | 28 |
| 2025 | 14 |
| 2026 so far | 5 |
Recent clearances
Newest MQV clearances in the FDA index, with applicant and decision date:
- K262230, Mg OSTEOREVIVE;Mg OSTEOCRETE, applicant Bone Solutions, Inc., decided 2026-09-11. FDA record
- K260364, Device 300419 Strip, applicant Geistlich Pharma AG, decided 2026-06-02. FDA record
- K252797, JAZBI Resorbable Bone Void Filler, applicant Sdip Innovations Pty, Ltd., decided 2026-05-26. FDA record
- K261008, Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute, applicant Stryker Spine, decided 2026-04-24. FDA record
- K253524, Adaptos®Fuse Bone Graft, applicant Biomendex OY, decided 2026-02-17. FDA record
- K253147, FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft Substitute FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute FIBERGRAFT BG Matrix Bone Graft Substitute, applicant Prosidyan, Inc., decided 2025-10-22. FDA record
- K251522, Mg OSTEOINJECT; Mg OSTEOREVIVE; Mg OSTEOCRETE, applicant Bone Solutions, Inc., decided 2025-10-13. FDA record
- K252085, Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom), applicant Wright Medical Technology, Inc. (Stryker Corporation), decided 2025-09-30. FDA record
What this means for a regulatory watcher
Volume tells you how deep the predicate pool is. A code with steady yearly counts gives you many candidate predicates, which helps when one predicate has a recall or design gap. A code with a sharp recent rise means reviewers are seeing more of this device type, so substantial equivalence arguments need to track the newest cleared devices, not five year old ones. Related device names in recent clearances include Device 300419 Strip, JAZBI Resorbable Bone Void Filler. Watch new MQV clearances as they post: each one is a possible predicate for your submission and a possible competitor worth reading.
FAQ
What is FDA product code MQV?
It is the three letter code FDA assigns to a device type in the 510(k) index. Recent MQV clearances include Mg OSTEOREVIVE;Mg OSTEOCRETE.
How many 510(k) clearances use product code MQV?
493 at the time this page was generated, from openFDA records.
How do I find a predicate device under MQV?
Start with the recent K numbers listed above, then run the free predicate search to check substantial equivalence text and review history.
How do I track new MQV clearances?
Get 510(k) alerts filtered to this product code and read each new clearance as it posts.
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Data: U.S. FDA via openFDA (public domain). Not regulatory advice. Assume all results are unvalidated.