FDA applicant

Binder Biomedical, Inc.

Boca Raton, FL2 decisions2010–20130 recalls

FDA records 2 decisions for Binder Biomedical, Inc. (Boca Raton, FL) from 2010 to 2013: 2 510(k) clearances. Most are in product codes MAX (Intervertebral Fusion Device With Bone Graft…) and OVD (Intervertebral Fusion Device With Integrated…). Its devices cite 5 predicates, 1 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 Binder Biomedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Binder Biomedical, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Binder Biomedical, Inc.’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 “Binder”

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

Binder GmbH 1

Binder Biomedical, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Binder”