FDA applicant

Alto Development Corp.

Farmingdale, NJ10 decisions1982–19962 recalls

FDA records 10 decisions for Alto Development Corp. (Farmingdale, NJ) from 1982 to 1996: 10 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and DRS (Transducer, Blood-Pressure, Extravascular). 2 recalls are 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 Alto Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alto Development Corp. since 2007.

Recalls per year

2in 2013

2007high 2 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Alto Development Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?