FDA applicant

Aquatemp Service Co., Inc.

Morristown, NJ1 decision1993–19930 recalls

FDA records 1 decision for Aquatemp Service Co., Inc. (Morristown, NJ) in 1993: 1 510(k) clearance. All are in product code KMY (Positioner, Tooth, Preformed). 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 Aquatemp Service Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aquatemp Service Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aquatemp Service Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?