FDA applicant

Lustgarten Multi-Tech International, Inc.

Framingham, MA3 decisions1988–19900 recalls

FDA records 3 decisions for Lustgarten Multi-Tech International, Inc. (Framingham, MA) from 1988 to 1990: 3 510(k) clearances. Most are in product codes EMA (Cement, Dental) and DZP (Instrument, Diamond, Dental). 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 Lustgarten Multi-Tech International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lustgarten Multi-Tech International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lustgarten Multi-Tech International, 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 “Lustgarten”

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

Lustgarten Multi-Tech Intl. 1

Lustgarten Multi-Tech International, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lustgarten”