FDA applicant

Servo Dental USA, Inc.

Northbrook, IL1 decision1999–19990 recalls

FDA records 1 decision for Servo Dental USA, Inc. (Northbrook, IL) in 1999: 1 510(k) clearance. All are in product code EIH (Powder, Porcelain). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Servo Dental USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Servo Dental USA, 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 “Servo”

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

Servo Med, Inc. 1

Servo Dental USA, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Servo”