FDA applicant

Biomet Osteobiologics

Warsaw, IN1 decision2007–20070 recalls

FDA records 1 decision for Biomet Osteobiologics (Warsaw, IN) in 2007: 1 510(k) clearance. All are in product code MQV (Filler, Bone Void, Calcium Compound). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Biomet Osteobiologics’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Biomet Osteobiologics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Biomet Osteobiologics’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Biomet”

FDA records each applicant name separately; these may or may not be the same firm.

Biomet, Inc. 446 Biomet Manufacturing Corp 129 Biomet Orthopedics, Inc. 41 Biomet 3i, Inc. 32 Biomet Microfixation 31 Biomet Spine 23 Biomet Sports Medicine 13 Biomet Spine (Aka Ebi, LLC) 13 Biomet Trauma 7 Biomet Trauma (Aka Ebi, Lp) 4 Biomet Micofixation 3 Biomet UK, Ltd. 3

Biomet Osteobiologics

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Biomet”