FDA applicant

Servo Med, Inc.

Greenwich, CT1 decision1984–19840 recalls

FDA records 1 decision for Servo Med, Inc. (Greenwich, CT) in 1984: 1 510(k) clearance. All are in product code GWN (Nystagmograph). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Servo Med, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Servo Med, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Servo”

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

Servo Dental USA, Inc. 1

Servo Med, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Servo”