FDA applicant

Cygnus Instruments, Inc.

Santa Barbara, CA2 decisions1990–19900 recalls

FDA records 2 decisions for Cygnus Instruments, Inc. (Santa Barbara, CA) in 1990: 2 510(k) clearances. Most are in product codes HRX (Arthroscope) and EHZ (Evacuator, Oral Cavity). 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, orthopedic panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cygnus 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 “Cygnus”

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

Cygnus Research Corp. 5 Cygnus of South Florida, Inc. 2 Cygnus, LLC 1

Cygnus Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cygnus”