FDA applicant

Bioceptive, Inc.

New Orleans, LA1 decision2014–20140 recalls

FDA records 1 decision for Bioceptive, Inc. (New Orleans, LA) in 2014: 1 510(k) clearance. All are in product code HDC (Tenaculum, Uterine). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

1in 2014

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Bioceptive, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Bioceptive, Inc.

Which product codes does it file in?

What has FDA decided for it lately?