FDA applicant

Lightspeed Endodontics

Houston, TX1 decision1993–19930 recalls

FDA records 1 decision for Lightspeed Endodontics (Houston, TX) in 1993: 1 510(k) clearance. All are in product code EKS (File, Pulp Canal, Endodontic). 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 Lightspeed Endodontics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lightspeed Endodontics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lightspeed”

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

Lightspeed Technology, Inc. 1

Lightspeed Endodontics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lightspeed”