510(k) Report

FDA applicant

Bryan Corp.

Woburn, MA5 decisions1986–20000 recalls

FDA records 5 decisions for Bryan Corp. (Woburn, MA) from 1986 to 2000: 5 510(k) clearances. Most are in product codes EOQ (Bronchoscope (Flexible Or Rigid)) and NWA (Prosthesis, Tracheal, Preformed/Molded). 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 Bryan Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bryan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bryan”

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