FDA applicant

Lite Specialty Metal Works, Inc.

Tualatin, OR1 decision1999–19990 recalls

FDA records 1 decision for Lite Specialty Metal Works, Inc. (Tualatin, OR) in 1999: 1 510(k) clearance. All are in product code EIA (Unit, Operative 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 Lite Specialty Metal Works, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lite Specialty Metal Works, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lite Specialty Metal Works, 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 “Lite”

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

Lite-Med, Inc. 3 Lite-On Technology Corp. H.S.P.B. 1

Lite Specialty Metal Works, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lite”