FDA applicant

Bioenterics Corp.

Carpinteria, CA4 decisions1992–20010 recalls

FDA records 4 decisions for Bioenterics Corp. (Carpinteria, CA) from 1992 to 2001: 4 510(k) clearances. Most are in product codes HMJ (Screen, Tangent, Projection, Battery-Powered) and FDG (Retractor, Fiberoptic). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Bioenterics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Bioenterics Corp.

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?