FDA applicant

Bio-Interfaces, Inc.

San Diego, CA17 decisions1989–19960 recalls

FDA records 17 decisions for Bio-Interfaces, Inc. (San Diego, CA) from 1989 to 1996: 17 510(k) clearances. Most are in product codes LYC (Bone Grafting Material, Synthetic) and EID (Syringe, Restorative And Impression Material). 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 Bio-Interfaces, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bio-Interfaces, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Bio-Interfaces, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?