FDA applicant

Biomimetic Therapeutics, LLC

Franklin1 decision2015–20151 recall

FDA records 1 decision for Biomimetic Therapeutics, LLC (Franklin) in 2015: 1 original PMA approval. All are in product code NOX (Filler, Bone Void, Synthetic Peptide). 1 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 Biomimetic Therapeutics, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

1in 2021

2015high 1 (2021) · low 0 (2015)2026

Class I Class II/III not classified

FIG. 1 — Biomimetic Therapeutics, LLC by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Biomimetic Therapeutics, LLC’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 “Biomimetic”

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

Biomimetic Pharmaceuticals, Inc. 1

Biomimetic Therapeutics, LLC

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Biomimetic”