FDA applicant

Biomet Interpore Cross

Irvine, CA1 decision2012–20120 recalls

FDA records 1 decision for Biomet Interpore Cross (Irvine, CA) in 2012: 1 510(k) clearance. All are in product code NUN (Bone Grafting Material, Human Source). Its devices cite 1 predicate, 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, dental panel, where it files most

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

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Biomet Interpore Cross by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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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 Interpore Cross

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”