FDA applicant

Minrad, Inc.

Orchard Park, NY14 decisions1997–20070 recalls

FDA records 14 decisions for Minrad, Inc. (Orchard Park, NY) from 1997 to 2007: 14 510(k) clearances. Most are in product codes KNW (Instrument, Biopsy) and CCW (Laryngoscope, Rigid). Its devices cite 4 predicates, 2 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, anesthesiology panel, where it files most

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

FDA decisions per year

2in 2007

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Minrad, 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?