FDA applicant

Concord Protex

Keene, NH1 decision1991–19910 recalls

FDA records 1 decision for Concord Protex (Keene, NH) in 1991: 1 510(k) clearance. All are in product code BSY (Catheters, Suction, Tracheobronchial). 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 Concord Protex’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Concord Protex since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Concord”

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

Concord Laboratories, Inc. 42 Concord/Portex 23 Concord Imaging, Ltd. 1 Concord Medical Products 1

Concord Protex

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Concord”