FDA applicant

Cavitron Surgical Systems

Stamford, CT1 decision1988–19880 recalls

FDA records 1 decision for Cavitron Surgical Systems (Stamford, CT) in 1988: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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 Cavitron Surgical Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cavitron Surgical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Cavitron”

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

Cavitron Corp. 32

Cavitron Surgical Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cavitron”