510(k) Report

FDA applicant

Ultralase Technologies, Inc.

Temple City, CA1 decision1996–19960 recalls

FDA records 1 decision for Ultralase Technologies, Inc. (Temple City, CA) in 1996: 1 510(k) clearance. All are in product code LFL (Instrument, Ultrasonic Surgical). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Ultralase Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ultralase Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ultralase Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LFLInstrument, Ultrasonic Surgical1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K960374Ultracut 2000Ultralase Technologies, Inc. · 1996

The one decision as Ultralase Technologies, Inc. →