FDA applicant

Falcon Instruments, Inc.

Bethesda, MD4 decisions1992–19930 recalls

FDA records 4 decisions for Falcon Instruments, Inc. (Bethesda, MD) from 1992 to 1993: 4 510(k) clearances. Most are in product codes MDM (Instrument, Manual, Surgical, General Use) and HRQ (Hemostat). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Falcon Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Falcon”

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

Falcon Medical Industries, Inc. 1

Falcon Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Falcon”